RU2012138257A - Замещенные пирролидин-2-карбоксамиды - Google Patents

Замещенные пирролидин-2-карбоксамиды Download PDF

Info

Publication number
RU2012138257A
RU2012138257A RU2012138257/04A RU2012138257A RU2012138257A RU 2012138257 A RU2012138257 A RU 2012138257A RU 2012138257/04 A RU2012138257/04 A RU 2012138257/04A RU 2012138257 A RU2012138257 A RU 2012138257A RU 2012138257 A RU2012138257 A RU 2012138257A
Authority
RU
Russia
Prior art keywords
fluorophenyl
chloro
dimethylpropyl
carbonyl
amino
Prior art date
Application number
RU2012138257/04A
Other languages
English (en)
Other versions
RU2564022C2 (ru
Inventor
Дейвид Джозеф БАРТКОВИЦ
Синьцзи Чу
Цинцзи Дин
Нань ЯН
Цзиньцзунь ЛЮ
Тина Морган РОСС
Цзин ЧЖАН
Чжумин ЧЖАН
Original Assignee
Ф.Хоффманн-Ля Рош Аг
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ф.Хоффманн-Ля Рош Аг filed Critical Ф.Хоффманн-Ля Рош Аг
Publication of RU2012138257A publication Critical patent/RU2012138257A/ru
Application granted granted Critical
Publication of RU2564022C2 publication Critical patent/RU2564022C2/ru

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/16Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Abstract

1. Соединение, выбранное из группы, включающейхиральный трет-бутиловый эфир [2-(4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-фенил)-этил]-карбаминовой кислоты,рац-трет-бутиловый эфир (4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-бензил)-карбаминовой кислоты,этиловый эфир 1-(4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-фенил)-пиперидин-4-карбоновой кислоты,1-(4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-фенил)-пиперидин-4-карбоновую кислоту,рац-трет-бутиловый эфир 4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-4-метилпиперидин-1-карбоновой кислоты,метиловый эфир 4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-3-трифторметоксибензойной кислоты,4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-3-трифторметоксибензойную кислоту,метиловый эфир 4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-3-метоксибензойной кислоты,метиловый эфир 4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циапо-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-3-фторбензойной кислоты,метиловый эфир 4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-3-хлорбензойной кислоты,4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметил�

Claims (9)

1. Соединение, выбранное из группы, включающей
хиральный трет-бутиловый эфир [2-(4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-фенил)-этил]-карбаминовой кислоты,
рац-трет-бутиловый эфир (4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-бензил)-карбаминовой кислоты,
этиловый эфир 1-(4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-фенил)-пиперидин-4-карбоновой кислоты,
1-(4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-фенил)-пиперидин-4-карбоновую кислоту,
рац-трет-бутиловый эфир 4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-4-метилпиперидин-1-карбоновой кислоты,
метиловый эфир 4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-3-трифторметоксибензойной кислоты,
4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-3-трифторметоксибензойную кислоту,
метиловый эфир 4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-3-метоксибензойной кислоты,
метиловый эфир 4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циапо-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-3-фторбензойной кислоты,
метиловый эфир 4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-3-хлорбензойной кислоты,
4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-3-хлорбензойную кислоту,
метиловый эфир 4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-2,5-дифторбензойной кислоты,
4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-2,5-дифторбензойную кислоту,
4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-2,6-дифторбензойную кислоту,
4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-3-гидроксибензойную кислоту,
метиловый эфир 4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-2-фтор-5-метоксибензойной кислоты,
4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-2-фтор-5-метоксибензойную кислоту,
рац-4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-2-этоксибензойную кислоту,
5-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-пиразин-2-карбоновую кислоту,
4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-3-метоксибензойную кислоту, и
4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-2-трифторметилбензойную кислоту, и
их фармацевтически приемлемые соли.
2. Соединение по п.1
Figure 00000001
рац-4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-2-этоксибензойная кислота.
3. Соединение по п.1
Figure 00000002
5-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-пиразин-2-карбоновая кислота.
4. Соединение по п.1
Figure 00000003
4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-3-метоксибензойная кислота.
5. Соединение по п.1
Figure 00000004
4-{[(2R,3S,4R,5S)-4-(4-хлор-2-фторфенил)-3-(3-хлор-2-фторфенил)-4-циано-5-(2,2-диметилпропил)-пирролидин-2-карбонил]-амино}-2-трифторметилбензойная кислота.
6. Фармацевтический препарат, содержащий соединение по любому из пп.1-5 вместе с фармацевтически приемлемыми инертными наполнителями или носителями.
7. Соединение по любому из пп.1-5, предназначенное для применения в качестве лекарственного средства.
8. Соединение по любому из пп.1-5, предназначенное для применения в качестве лекарственного средства, предназначенного для лечения рака, предпочтительно солидных опухолей, более предпочтительно опухолей молочной железы, толстой кишки, легких и предстательной железы.
9. Применение соединения по любому из пп.1-5 для приготовления лекарственного средства, предназначенного для лечения рака, предпочтительно солидных опухолей, более предпочтительно.
RU2012138257/04A 2010-02-09 2011-02-04 Замещенные пирролидин-2-карбоксамиды RU2564022C2 (ru)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US12/702,402 US8354444B2 (en) 2008-09-18 2010-02-09 Substituted pyrrolidine-2-carboxamides
US12/702,402 2010-02-09
PCT/EP2011/051619 WO2011098398A1 (en) 2010-02-09 2011-02-04 Substituted pyrrolidine-2-carboxamides

Publications (2)

Publication Number Publication Date
RU2012138257A true RU2012138257A (ru) 2014-03-20
RU2564022C2 RU2564022C2 (ru) 2015-09-27

Family

ID=43608850

Family Applications (1)

Application Number Title Priority Date Filing Date
RU2012138257/04A RU2564022C2 (ru) 2010-02-09 2011-02-04 Замещенные пирролидин-2-карбоксамиды

Country Status (32)

Country Link
US (1) US8354444B2 (ru)
EP (1) EP2534132B1 (ru)
JP (1) JP5612710B2 (ru)
KR (1) KR101461298B1 (ru)
CN (1) CN102753522B (ru)
AR (2) AR080143A1 (ru)
AU (1) AU2011214506C1 (ru)
BR (1) BR112012019672B1 (ru)
CA (1) CA2788236C (ru)
CL (1) CL2012002189A1 (ru)
CR (1) CR20120410A (ru)
CY (1) CY1119049T1 (ru)
DK (1) DK2534132T3 (ru)
EC (1) ECSP12012083A (ru)
ES (1) ES2629439T3 (ru)
HK (1) HK1171452A1 (ru)
HR (1) HRP20170903T1 (ru)
HU (1) HUE034816T2 (ru)
LT (1) LT2534132T (ru)
MX (1) MX2012009186A (ru)
MY (1) MY165238A (ru)
NZ (1) NZ601422A (ru)
PE (1) PE20121532A1 (ru)
PL (1) PL2534132T3 (ru)
PT (1) PT2534132T (ru)
RS (1) RS56163B1 (ru)
RU (1) RU2564022C2 (ru)
SG (1) SG182763A1 (ru)
SI (1) SI2534132T1 (ru)
TW (1) TWI401243B (ru)
UA (1) UA107954C2 (ru)
WO (1) WO2011098398A1 (ru)

Families Citing this family (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7303676B2 (en) * 2003-02-13 2007-12-04 Zenon Technology Partnership Supported biofilm apparatus and process
GB0811643D0 (en) 2008-06-25 2008-07-30 Cancer Rec Tech Ltd New therapeutic agents
US8354444B2 (en) 2008-09-18 2013-01-15 Hoffmann-La Roche Inc. Substituted pyrrolidine-2-carboxamides
US8859776B2 (en) 2009-10-14 2014-10-14 Merck Sharp & Dohme Corp. Substituted piperidines that increase p53 activity and the uses thereof
US8088815B2 (en) * 2009-12-02 2012-01-03 Hoffman-La Roche Inc. Spiroindolinone pyrrolidines
US20120010235A1 (en) * 2010-07-12 2012-01-12 Xin-Jie Chu N-substituted pyrrolidines
US8709419B2 (en) 2010-08-17 2014-04-29 Hoffmann-La Roche, Inc. Combination therapy
US9295669B2 (en) 2010-12-14 2016-03-29 Hoffman La-Roche Inc. Combination therapy for proliferative disorders
JP5792279B2 (ja) 2011-03-10 2015-10-07 第一三共株式会社 ジスピロピロリジン誘導体
EP2771008A4 (en) 2011-10-28 2015-04-08 Merck Sharp & Dohme MACROCYCLES INCREASING P53 ACTIVITY AND USES THEREOF
EP2793890B1 (en) 2011-12-21 2016-09-07 Merck Sharp & Dohme Corp. Substituted piperidines as hdm2 inhibitors
US8993614B2 (en) 2012-03-15 2015-03-31 F. Hoffmann-La Roche Ag Substituted pyrrolidine-2-carboxamides
US9216170B2 (en) * 2012-03-19 2015-12-22 Hoffmann-La Roche Inc. Combination therapy for proliferative disorders
US20140200255A1 (en) * 2012-03-19 2014-07-17 Brian Higgins Method for administration
US20130245089A1 (en) * 2012-03-19 2013-09-19 Hoffmann-La Roche Inc. Method for administration
RU2014150492A (ru) 2012-05-30 2016-07-20 Ф. Хоффманн-Ля Рош Аг Замещенные пирролидин-2-карбоксамиды
TWI586668B (zh) 2012-09-06 2017-06-11 第一三共股份有限公司 二螺吡咯啶衍生物之結晶
WO2014100065A1 (en) 2012-12-20 2014-06-26 Merck Sharp & Dohme Corp. Substituted imidazopyridines as hdm2 inhibitors
BR112015015758B1 (pt) * 2013-01-22 2022-01-04 F. Hoffmann-La Roche Ag Dispersão sólida, formulação sólida de dose unitária, preparação farmacêutica e uso de uma dispersão sólida
US9828340B2 (en) * 2013-02-21 2017-11-28 Hoffmann-La Roche Inc. Asymmetric synthesis of a substituted pyrrolidine-2-carboxamide
US20140275562A1 (en) * 2013-03-13 2014-09-18 Dow Agrosciences Llc Preparation of certain (substituted phenyl)-triazolyl-(substituted phenyl) molecules, and intermediates and insecticides related thereto
BR112015030734A2 (pt) * 2013-06-19 2017-07-25 Hoffmann La Roche produto farmacêutico, kit e método de tratamento
US20160129033A1 (en) * 2013-06-19 2016-05-12 Hoffmann-La Roche Inc. Combination of ro5503781 and capecitabine for cancer therapy
WO2014206866A1 (en) * 2013-06-24 2014-12-31 F. Hoffmann-La Roche Ag Stable intravenous formulation
KR101879926B1 (ko) 2013-07-03 2018-08-16 에프. 호프만-라 로슈 아게 MDM2 길항제를 사용한 환자 암 치료를 개인화하기 위한 mRNA-기반 유전자 발현
SI3077004T1 (sl) 2013-12-05 2020-07-31 F. Hoffmann-La Roche Ag Novo kombinirano zdravilo za akutno mieloično levkemijo (AML)
US9657351B2 (en) 2013-12-06 2017-05-23 Hoffman-La Roche Inc. MRNA-based gene expression for personalizing patient cancer therapy with an MDM2 antagonist
EP3131878A1 (en) * 2014-04-15 2017-02-22 F. Hoffmann-La Roche AG Solid forms of a pharmaceutically active compound
ES2712973T3 (es) 2014-04-17 2019-05-17 Univ Michigan Regents Inhibidores de MDM2 y métodos terapéuticos que usan los mismos
JP6162646B2 (ja) * 2014-05-27 2017-07-12 信越化学工業株式会社 3,5−ジメチルドデカン酸の製造方法
WO2016055497A1 (en) * 2014-10-10 2016-04-14 F. Hoffmann-La Roche Ag Methods for personalizing patient cancer therapy with an mdm2 antagonist
SG11201706542TA (en) * 2015-03-30 2017-10-30 Mission Therapeutics Ltd 1-cyano-pyrrolidine compounds as usp30 inhibitors
GB201517217D0 (en) 2015-09-29 2015-11-11 Astex Therapeutics Ltd And Cancer Res Technology Ltd Pharmaceutical compounds
GB201517216D0 (en) 2015-09-29 2015-11-11 Cancer Res Technology Ltd And Astex Therapeutics Ltd Pharmaceutical compounds
ES2858151T3 (es) 2016-05-20 2021-09-29 Hoffmann La Roche Conjugados de PROTAC-anticuerpo y procedimientos de uso
KR102122469B1 (ko) 2016-11-01 2020-06-12 주식회사 엘지화학 변성 공액디엔계 중합체 및 이의 제조방법
CA3048088C (en) 2016-12-30 2021-05-04 Oriental (Luzhou) Agrochemicals. Co., Ltd. Method for preparing 2-(cyclohexenylidene) malonic acid derivatives and uses thereof
GB201704965D0 (en) 2017-03-28 2017-05-10 Astex Therapeutics Ltd Pharmaceutical compounds
GB201704966D0 (en) 2017-03-28 2017-05-10 Astex Therapeutics Ltd Pharmaceutical compounds
SG11202000230VA (en) 2017-07-11 2020-02-27 Vertex Pharma Carboxamides as modulators of sodium channels
CN108586195A (zh) * 2017-12-27 2018-09-28 北京汇康博源医药科技有限公司 一种5-羟基-7,7-二甲基-2h-茚酮的制备方法
WO2019213106A1 (en) 2018-04-30 2019-11-07 Teva Pharmaceuticals International Gmbh Solid state forms of idasanutlin
KR20220124176A (ko) 2019-12-06 2022-09-13 버텍스 파마슈티칼스 인코포레이티드 나트륨 채널의 조절제로서의 치환된 테트라하이드로푸란
KR20240031300A (ko) 2021-06-04 2024-03-07 버텍스 파마슈티칼스 인코포레이티드 나트륨 채널 조절제로서의 n-(하이드록시알킬 (헤테로)아릴) 테트라하이드로푸란 카르복스아미드
WO2023056069A1 (en) 2021-09-30 2023-04-06 Angiex, Inc. Degrader-antibody conjugates and methods of using same
CN116459225B (zh) * 2023-04-26 2023-11-10 东莞市金美济药业有限公司 一种艾拉戈克钠片及其制备工艺

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4732902A (en) 1986-05-23 1988-03-22 Hoffmann-La Roche Inc. Pyrroloisoquinolinyl-dimethyloxoalkyl alkonoates and their use as antipsychotic agents
TW394760B (en) 1993-09-07 2000-06-21 Hoffmann La Roche Novel Carboxamides, process for their preparation and pharmaceutical composition containing the same
CA2298601A1 (en) 1997-08-28 1999-03-11 Pharmacia & Upjohn Company Inhibitors of protein tyrosine phosphatase
US6482921B1 (en) 1999-01-28 2002-11-19 Essential Therapeutics, Inc. Uridyl peptide antibiotic (UPA) derivatives, their synthesis and use
US6531494B1 (en) 2001-08-29 2003-03-11 Pharmacia Corporation Gem-substituted αvβ3 antagonists
US6916833B2 (en) * 2003-03-13 2005-07-12 Hoffmann-La Roche Inc. Substituted piperidines
CN1294120C (zh) * 2003-10-21 2007-01-10 山东大学 吡咯烷类基质金属蛋白酶抑制剂及其应用
US7550487B2 (en) * 2004-03-26 2009-06-23 Hoffmann-La Roche Inc. Pyrrolidine-3,4-dicarboxamide derivatives
SG176463A1 (en) * 2005-02-22 2011-12-29 Univ Michigan Small molecule inhibitors of mdm2 and uses thereof
EA014445B1 (ru) 2005-02-22 2010-12-30 Дзе Риджентс Оф Дзе Юниверсити Оф Мичиган Низкомолекулярные ингибиторы mdm2 и их применения
CN101243069A (zh) 2005-06-17 2008-08-13 阿斯利康(瑞典)有限公司 凝血酶抑制剂2-氧代-1,2,5,6-四氢吡啶衍生物
US7884107B2 (en) 2006-06-30 2011-02-08 Merck Substituted piperidines that increase P53 activity and the uses thereof
RU2459619C2 (ru) 2006-12-06 2012-08-27 Санофи-Авентис Мочевина и сульфамидные производные в качестве ингибиторов tafia
TW200911787A (en) 2007-07-03 2009-03-16 Astrazeneca Ab New aza-bicyclohexane compounds useful as inhibitors of thrombin
JO2704B1 (en) * 2007-09-21 2013-03-03 جانسين فارماسوتيكا ان في Interference inhibition factors between MD2 and B53
US8134001B2 (en) * 2007-12-14 2012-03-13 Hoffmann-La Roche Inc. Spiroindolinone derivatives
KR101673886B1 (ko) 2008-06-06 2016-11-08 사노피 TAFIa의 억제제로서의 마크로사이클릭 우레아 및 술파미드 유도체
EP2321301A4 (en) 2008-06-23 2011-09-28 Astrazeneca Ab NOVEL HETEROCYCLIC CARBOXAMIDES AS THROMBIN INHIBITORS
GB0811643D0 (en) * 2008-06-25 2008-07-30 Cancer Rec Tech Ltd New therapeutic agents
JP5658157B2 (ja) 2008-09-18 2015-01-21 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft 置換ピロリジン−2−カルボキサミド
US8354444B2 (en) 2008-09-18 2013-01-15 Hoffmann-La Roche Inc. Substituted pyrrolidine-2-carboxamides
US8017607B2 (en) 2009-10-14 2011-09-13 Hoffmann-La Roche Inc. N-substituted-pyrrolidines as inhibitors of MDM2-P-53 interactions

Also Published As

Publication number Publication date
RS56163B1 (sr) 2017-11-30
US8354444B2 (en) 2013-01-15
CR20120410A (es) 2012-09-05
MY165238A (en) 2018-03-14
PT2534132T (pt) 2017-06-26
JP2013518921A (ja) 2013-05-23
TWI401243B (zh) 2013-07-11
KR20120119922A (ko) 2012-10-31
SG182763A1 (en) 2012-08-30
BR112012019672A2 (pt) 2016-05-03
CL2012002189A1 (es) 2012-11-23
EP2534132A1 (en) 2012-12-19
AR080143A1 (es) 2012-03-14
PL2534132T3 (pl) 2017-09-29
HK1171452A1 (en) 2013-03-28
JP5612710B2 (ja) 2014-10-22
AU2011214506B2 (en) 2014-04-17
BR112012019672B1 (pt) 2020-11-17
MX2012009186A (es) 2012-08-23
HUE034816T2 (en) 2018-02-28
DK2534132T3 (en) 2017-07-10
CA2788236C (en) 2015-01-20
HRP20170903T1 (hr) 2017-09-08
ECSP12012083A (es) 2012-09-28
CN102753522B (zh) 2013-11-27
CA2788236A1 (en) 2011-08-18
NZ601422A (en) 2014-07-25
AU2011214506C1 (en) 2014-07-17
EP2534132B1 (en) 2017-04-26
WO2011098398A1 (en) 2011-08-18
SI2534132T1 (sl) 2017-08-31
US20100152190A1 (en) 2010-06-17
KR101461298B1 (ko) 2014-11-28
ES2629439T3 (es) 2017-08-09
CN102753522A (zh) 2012-10-24
AR114159A2 (es) 2020-07-29
TW201136892A (en) 2011-11-01
CY1119049T1 (el) 2018-01-10
UA107954C2 (en) 2015-03-10
RU2564022C2 (ru) 2015-09-27
PE20121532A1 (es) 2012-11-26
AU2011214506A1 (en) 2012-08-16
LT2534132T (lt) 2017-07-10

Similar Documents

Publication Publication Date Title
RU2012138257A (ru) Замещенные пирролидин-2-карбоксамиды
ES2925564T3 (es) Derivados de azetidina tal como moduladores de receptores de quimiocinas y usos de los mismos
RU2494095C2 (ru) Модифицированные миметики лизина
NZ631477A (en) Substituted pyrrolidine-2-carboxamides
MX2021013472A (es) Moduladores de thr-? y metodos de uso de estos.
CN1101392C (zh) 抑制法呢基蛋白质转移酶的(咪唑-5-基)甲基-2-喹啉酮衍生物
RU2498988C2 (ru) Ингибиторы активности протеинтирозинкиназы
TW201841896A (zh) 作為pd—l1抑制劑的雜環類化合物
RU2008137526A (ru) Ингибиторы киназы, основанные на гидантоине
RU2008112683A (ru) Ингибиторы fap
PE20141824A1 (es) Compuestos terapeuticamente activos y sus metodos de uso
PE20141075A1 (es) 4-aril-n-fenil-1,3,5-triazin-2-aminas que contienen un grupo sulfoximina
EA201270546A1 (ru) ЗАМЕЩЕННЫЕ ПИПЕРИДИНЫ, КОТОРЫЕ ПОВЫШАЮТ АКТИВНОСТЬ p53, И ИХ ПРИМЕНЕНИЕ
EA201591753A1 (ru) 3-пиримидин-4-илоксазолидин-2-оны в качестве ингибиторов мутантного idh
NZ594177A (en) Novel benzodiazepine derivatives
NZ626505A (en) Substituted pyrrolidine-2-carboxamides
MX2010004501A (es) Inhibidor de la proteina de activacion de 5-lipoxigenasa (plap).
RU2011144763A (ru) 6-(3-азабицикло[3.1.0]гекс-3-ил)-2-фенилпиримидины
EA201491007A1 (ru) Лекарственные составы
EA200901573A1 (ru) Гетероарилзамещенные тиазолы
PE20050011A1 (es) Compuesto de difenilazetidinona con propiedades fisiologicas mejoradas, procedimiento para su preparacion y medicamentos que comprenden este compuesto
JP2006501201A5 (ru)
PE20081703A1 (es) Nuevos derivados triciclicos, su procedimiento de preparacion y las composiciones farmaceuticas que los contienen
EA201270266A1 (ru) Гетероциклические соединения
CN102131775A (zh) 雄激素受体n-末端活化的小分子抑制剂