DD144768A5 - Verfahren zur herstellung von 3-benzyl-3-azabicyclo eckige klammer auf 3,1,0 eckige klammer zu hexan - Google Patents

Verfahren zur herstellung von 3-benzyl-3-azabicyclo eckige klammer auf 3,1,0 eckige klammer zu hexan Download PDF

Info

Publication number: DD144768A5
Authority: DD; German Democratic Republic
Prior art keywords: benzyl; azabicyclo; hexane; item; temperature
Prior art date: 1978-07-06

Application number

DD79214104A

Other languages

German (de)

English (en)

Inventor

Willy D Kollmeyer

Original Assignee

Shell Int Research

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.)

1978-07-06

Filing date

1979-07-04

Publication date

1980-11-05

1979-07-04 Application filed by Shell Int Research filed Critical Shell Int Research

1980-11-05 Publication of DD144768A5 publication Critical patent/DD144768A5/de

Links

VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 title claims abstract description 31
238000004519 manufacturing process Methods 0.000 title 1
150000001875 compounds Chemical class 0.000 claims abstract description 9
-1 Carboxy TM 3 Chemical compound 0.000 claims abstract description 7
238000002360 preparation method Methods 0.000 claims abstract description 5
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims abstract description 3
AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims abstract 2
238000006243 chemical reaction Methods 0.000 claims description 23
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
238000000034 method Methods 0.000 claims description 14
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 10
150000008064 anhydrides Chemical class 0.000 claims description 10
WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 claims description 10
239000003638 chemical reducing agent Substances 0.000 claims description 10
239000003054 catalyst Substances 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
238000007327 hydrogenolysis reaction Methods 0.000 claims description 4
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
229910052708 sodium Inorganic materials 0.000 claims description 3
239000011734 sodium Substances 0.000 claims description 3
229910052763 palladium Inorganic materials 0.000 claims description 2
ZTHPDQRRMAKLIQ-UHFFFAOYSA-N 2-[1-(carboxymethyl)cyclopropyl]acetic acid Chemical compound OC(=O)CC1(CC(O)=O)CC1 ZTHPDQRRMAKLIQ-UHFFFAOYSA-N 0.000 claims 1
150000001942 cyclopropanes Chemical class 0.000 claims 1
239000012280 lithium aluminium hydride Substances 0.000 claims 1
230000004071 biological effect Effects 0.000 abstract description 2
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 42
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 27
239000000203 mixture Substances 0.000 description 17
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 16
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
239000002904 solvent Substances 0.000 description 11
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
238000009835 boiling Methods 0.000 description 10
239000000047 product Substances 0.000 description 10
239000000243 solution Substances 0.000 description 9
239000002253 acid Substances 0.000 description 8
238000001816 cooling Methods 0.000 description 8
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
238000002844 melting Methods 0.000 description 6
230000008018 melting Effects 0.000 description 6
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
238000004821 distillation Methods 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
239000012043 crude product Substances 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
238000001914 filtration Methods 0.000 description 4
238000010438 heat treatment Methods 0.000 description 4
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
238000005481 NMR spectroscopy Methods 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
239000006227 byproduct Substances 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
239000007789 gas Substances 0.000 description 3
239000011521 glass Substances 0.000 description 3
229930195733 hydrocarbon Natural products 0.000 description 3
150000002430 hydrocarbons Chemical class 0.000 description 3
239000010410 layer Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
239000003921 oil Substances 0.000 description 3
239000012044 organic layer Substances 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
238000010992 reflux Methods 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
238000003756 stirring Methods 0.000 description 3
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
239000004215 Carbon black (E152) Substances 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
229960000583 acetic acid Drugs 0.000 description 2
238000009903 catalytic hydrogenation reaction Methods 0.000 description 2
125000004122 cyclic group Chemical group 0.000 description 2
VEUUMBGHMNQHGO-UHFFFAOYSA-N ethyl chloroacetate Chemical compound CCOC(=O)CCl VEUUMBGHMNQHGO-UHFFFAOYSA-N 0.000 description 2
235000019253 formic acid Nutrition 0.000 description 2
230000006698 induction Effects 0.000 description 2
229910052744 lithium Inorganic materials 0.000 description 2
239000000463 material Substances 0.000 description 2
239000002480 mineral oil Substances 0.000 description 2
235000010446 mineral oil Nutrition 0.000 description 2
239000000376 reactant Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
238000002390 rotary evaporation Methods 0.000 description 2
239000012312 sodium hydride Substances 0.000 description 2
229910000104 sodium hydride Inorganic materials 0.000 description 2
229910052938 sodium sulfate Inorganic materials 0.000 description 2
235000011152 sodium sulphate Nutrition 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
RLWFMZKPPHHHCB-WSOKHJQSSA-N (1r,2s)-cyclopropane-1,2-dicarboxylic acid Chemical compound OC(=O)[C@H]1C[C@H]1C(O)=O RLWFMZKPPHHHCB-WSOKHJQSSA-N 0.000 description 1
DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 1
HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 description 1
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000004280 Sodium formate Substances 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
230000002411 adverse Effects 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000000538 analytical sample Substances 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
238000010533 azeotropic distillation Methods 0.000 description 1
239000002585 base Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
235000013351 cheese Nutrition 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
FDKLLWKMYAMLIF-UHFFFAOYSA-N cyclopropane-1,1-dicarboxylic acid Chemical compound OC(=O)C1(C(O)=O)CC1 FDKLLWKMYAMLIF-UHFFFAOYSA-N 0.000 description 1
230000018044 dehydration Effects 0.000 description 1
238000006297 dehydration reaction Methods 0.000 description 1
238000006356 dehydrogenation reaction Methods 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
230000008034 disappearance Effects 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000000284 extract Substances 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000004508 fractional distillation Methods 0.000 description 1
239000012362 glacial acetic acid Substances 0.000 description 1
150000004678 hydrides Chemical class 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
239000003999 initiator Substances 0.000 description 1
239000002198 insoluble material Substances 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
238000002955 isolation Methods 0.000 description 1
229910052987 metal hydride Inorganic materials 0.000 description 1
150000004681 metal hydrides Chemical class 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910000510 noble metal Inorganic materials 0.000 description 1
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
239000000523 sample Substances 0.000 description 1
238000007127 saponification reaction Methods 0.000 description 1
239000002002 slurry Substances 0.000 description 1
HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 1
235000019254 sodium formate Nutrition 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
239000012258 stirred mixture Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
239000000052 vinegar Substances 0.000 description 1
235000021419 vinegar Nutrition 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/52—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring condensed with a ring other than six-membered
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/09—Preparation of carboxylic acids or their salts, halides or anhydrides from carboxylic acid esters or lactones
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/54—Preparation of carboxylic acid anhydrides
- C07C51/56—Preparation of carboxylic acid anhydrides from organic acids, their salts, their esters or their halides, e.g. by carboxylation

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Oil, Petroleum & Natural Gas (AREA)
Indole Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DD79214104A 1978-07-06 1979-07-04 Verfahren zur herstellung von 3-benzyl-3-azabicyclo eckige klammer auf 3,1,0 eckige klammer zu hexan DD144768A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/922,407 US4183857A (en)	1978-07-06	1978-07-06	3-Benzyl-3-azabicyclo(3.1.0)hexane-2,4-dione

Publications (1)

Publication Number	Publication Date
DD144768A5 true DD144768A5 (de)	1980-11-05

Family

ID=25446984

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79214104A DD144768A5 (de)	1978-07-06	1979-07-04	Verfahren zur herstellung von 3-benzyl-3-azabicyclo eckige klammer auf 3,1,0 eckige klammer zu hexan

Country Status (15)

Country	Link
US (1)	US4183857A (xx)
EP (1)	EP0007128B1 (xx)
JP (1)	JPS5511587A (xx)
AU (1)	AU527833B2 (xx)
BR (1)	BR7904218A (xx)
CA (1)	CA1116612A (xx)
CS (1)	CS210692B2 (xx)
DD (1)	DD144768A5 (xx)
DE (1)	DE2964802D1 (xx)
DK (1)	DK240979A (xx)
ES (1)	ES482177A1 (xx)
IL (1)	IL57718A0 (xx)
PL (1)	PL116900B1 (xx)
SU (1)	SU969158A3 (xx)
ZA (1)	ZA793334B (xx)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1116617A (en) *	1978-12-14	1982-01-19	Janet A. Day	Esters of 2-carboxy-3-azabicyclo¬3.1.0\|hex-2-ene
US5256791A (en) *	1992-03-02	1993-10-26	Pfizer Inc.	Preparation of intermediates in the synthesis of quinoline antibiotics
GB9620049D0 (en) *	1996-09-26	1996-11-13	Hayles J R	Repellent formulations
US6395767B2 (en)	2000-03-10	2002-05-28	Bristol-Myers Squibb Company	Cyclopropyl-fused pyrrolidine-based inhibitors of dipeptidyl peptidase IV and method
WO2004014853A1 (en) *	2002-07-31	2004-02-19	Ranbaxy Laboratories Limited	3,6-disubstituted azabicyclo [3.1.0]hexane derivatives useful as muscarinic receptor antagonists
AU2002321711A1 (en) *	2002-08-09	2004-02-25	Ranbaxy Laboratories Limited	3,6-disubstituted azabicyclo (3.1.0) hexane derivatives useful as muscarinic receptor antagonist
US6875784B2 (en) *	2002-10-09	2005-04-05	Pharmacia & Upjohn Company	Antimibicrobial [3.1.0.] bicyclic oxazolidinone derivatives
ATE466007T1 (de) *	2005-11-30	2010-05-15	Hoffmann La Roche	5-substituierte indol-2-carbonsäureamidderivate
CA2634397A1 (en) *	2005-12-22	2007-07-05	Schering Corporation	Process for the preparation of 6,6-dimethyl-3-azabicyclo[3.1.0\|-hexane compounds and enantiomeric salts thereof
US8158807B2 (en) *	2006-12-20	2012-04-17	Schering Corporation	Process for the preparation of 6,6-dimethyl-3-azabicyclo-[3.1.0]-hexane compounds utilizing bisulfite intermediate
MX2010014500A (es)	2008-06-24	2011-05-30	Codexis Inc	Procedimientos biocataliticos para la preparacion de compuestos de prolina biciclica fusionada sustancialmente estereomericamente puros.
CN102432525A (zh) *	2011-10-20	2012-05-02	苏州康润医药有限公司	3-苄基-3-氮杂二环[2,1,0]己烷的实用合成方法
CN108341766B (zh) *	2017-01-24	2020-08-14	南京药石科技股份有限公司	一种3-氮杂双环[3.1.0]己烷盐酸盐的制备方法
JP7448331B2 (ja)	2019-10-09	2024-03-12	株式会社京都製作所	判定装置、封緘システム、推定モデル、生成装置、判定方法、封緘方法、及び生成方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3418336A (en) *	1965-04-02	1968-12-24	Tri Kem Corp	gem - cyclohexane - 1,1 - diacetic and-1-carboxy-1-acetic acids and their anhydrides
US3745170A (en) *	1969-03-19	1973-07-10	Sumitomo Chemical Co	Novel n-(3,5-dihalophenyl)-imide compounds
US3654305A (en) *	1970-01-26	1972-04-04	Robins Co Inc A H	5-azaspiro(2.4)heptanes
YU40105B (en) *	1973-07-04	1985-08-31	Science Union & Cie	Process for the manufacture of n-arylsulfonyl-n'-(aza-3-bicycloalyl)-carbamides
US4088652A (en) *	1975-07-31	1978-05-09	American Cyanamid Company	Acylazabicyclohexanes
JPS5247918A (en) *	1975-10-15	1977-04-16	Sumitomo Chem Co Ltd	Non-medical fungicides and method of making the same
GR72713B (xx) *	1976-09-15	1983-12-01	American Cyanamid Co

1978
- 1978-07-06 US US05/922,407 patent/US4183857A/en not_active Expired - Lifetime
1979
- 1979-06-08 DK DK240979A patent/DK240979A/da not_active Application Discontinuation
- 1979-06-14 CA CA000329751A patent/CA1116612A/en not_active Expired
- 1979-06-27 EP EP79200347A patent/EP0007128B1/en not_active Expired
- 1979-06-27 DE DE7979200347T patent/DE2964802D1/de not_active Expired
- 1979-07-04 CS CS794719A patent/CS210692B2/cs unknown
- 1979-07-04 BR BR7904218A patent/BR7904218A/pt unknown
- 1979-07-04 ZA ZA793334A patent/ZA793334B/xx unknown
- 1979-07-04 JP JP8404979A patent/JPS5511587A/ja active Pending
- 1979-07-04 PL PL1979216848A patent/PL116900B1/pl unknown
- 1979-07-04 SU SU792783601A patent/SU969158A3/ru active
- 1979-07-04 AU AU48636/79A patent/AU527833B2/en not_active Ceased
- 1979-07-04 DD DD79214104A patent/DD144768A5/de unknown
- 1979-07-04 ES ES482177A patent/ES482177A1/es not_active Expired
- 1979-07-04 IL IL57718A patent/IL57718A0/xx unknown

Also Published As

Publication number	Publication date
ZA793334B (en)	1980-06-25
PL216848A1 (xx)	1980-03-24
IL57718A0 (en)	1979-11-30
CA1116612A (en)	1982-01-19
DE2964802D1 (en)	1983-03-24
AU527833B2 (en)	1983-03-24
DK240979A (da)	1980-01-07
ES482177A1 (es)	1980-06-16
AU4863679A (en)	1980-01-10
SU969158A3 (ru)	1982-10-23
EP0007128A1 (en)	1980-01-23
JPS5511587A (en)	1980-01-26
BR7904218A (pt)	1981-01-05
PL116900B1 (en)	1981-07-31
CS210692B2 (en)	1982-01-29
US4183857A (en)	1980-01-15
EP0007128B1 (en)	1983-02-16

Publication	Publication Date	Title
DD144768A5 (de)	1980-11-05	Verfahren zur herstellung von 3-benzyl-3-azabicyclo eckige klammer auf 3,1,0 eckige klammer zu hexan
DE2004038C3 (de)	1982-03-25	5-Cyclohexyl-1-indancarbonsäuren,,deren Niedrigalkyl- und tert.-Aminoniedrigalkylester, nicht-toxische pharmakologisch verträgliche Salze und Verfahren zu deren Herstellung
DE2527289A1 (de)	1976-01-29	Verfahren zur herstellung von alkylacetophenonen
EP0061015B1 (de)	1984-04-11	Verfahren zur Herstellung eines 2-Alkylphenols
CH644579A5 (de)	1984-08-15	Verfahren zum cyclisieren von gamma-chlorcarbonsaeureestern.
DE2918900A1 (de)	1979-11-22	Verfahren zur herstellung von 1,5- dimethyl-bicyclo- eckige klammer auf 3,2,1 eckige klammer zu octanol-8 und dessen ester
DE69109791T2 (de)	1995-09-14	Verfahren zur Herstellung von Monohalogenalkanoylferrocenen.
EP0760367A2 (de)	1997-03-05	Verfahren zur Herstellung von 4-Acylamino-2,2,6,6-tetramethylpiperidinen
DE2716773A1 (de)	1977-11-03	Verfahren zur herstellung von estern von m-phenoxybenzylalkohol und seiner alpha-cyano- und alpha- aethinylderivate mit carbonsaeuren
DE3437634A1 (de)	1986-04-17	Verfahren zur herstellung von gegebenenfalls substituierter zimtsaeure in gegenwart eines katalysators
ACREE JR et al.	1937	Constituents of pyrethrum flowers. X. Identification of the fatty acids combined with pyrethrolone
DE2164662A1 (de)	1972-07-27	Indanderivate und Verfahren zu ihrer Herstellung
CA1127159A (en)	1982-07-06	Derivatives of 3-azabicyclo(3.1.0)hexane and processes for their preparation
EP0128489B1 (de)	1989-11-29	Verfahren zur Herstellung von Succinylobernsteinsäuredialkylestern
DE3874166T2 (de)	1993-03-25	Verfahren zum herstellen und isolieren von estern der (r)-2-hydroxyphenylbuttersaeure.
DE2738016C3 (de)	1981-06-04	Verfahren zur Herstellung von &alpha;-Keto-carbonsäuren und Keto-carbonsäureamiden als dafür geeignete Zwischenprodukte
DE3237646C2 (xx)	1991-10-10
DE2446753C2 (de)	1982-04-22	Verfahren zur Herstellung von äthylenisch ungesättigten Dicarbonsäuredialkylestern
DE3529159A1 (de)	1986-02-27	Neues verfahren zur herstellung eines aminolactons
DE2243305C3 (de)	1976-04-22	Neue Derivate von Phenylessigsäure, Verfahren zu ihrer Herstellung und pharmazeutische Zubereitungen, die die Derivate als Wirkstoff enthalten
CH626867A5 (en)	1981-12-15	Process for preparing 3,7-dialkylalkan-7-ol-1-als
DE2139084B2 (de)	1978-06-29	Verfahren zur Herstellung von 4,4-Diphenyl-piperidinen
DE2260447C3 (de)	1976-12-23	Verfahren zur Herstellung von Methyljasmonat
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