GB882537A - Chromones and processes for the preparation thereof - Google Patents

Chromones and processes for the preparation thereof

Info

Publication number
GB882537A
GB882537A GB31111/59A GB3111159A GB882537A GB 882537 A GB882537 A GB 882537A GB 31111/59 A GB31111/59 A GB 31111/59A GB 3111159 A GB3111159 A GB 3111159A GB 882537 A GB882537 A GB 882537A
Authority
GB
United Kingdom
Prior art keywords
solvent
concentrating
residue
alkyl
under vacuum
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
GB31111/59A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Recordati Laboratorio Farmacologico SpA
Original Assignee
Recordati Laboratorio Farmacologico SpA
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 Recordati Laboratorio Farmacologico SpA filed Critical Recordati Laboratorio Farmacologico SpA
Publication of GB882537A publication Critical patent/GB882537A/en
Expired legal-status Critical Current

Links

Abstract

The invention comprises compounds of general formula <FORM:0882537/IV (b)/1> in which <FORM:0882537/IV (b)/2> R2 is alkyl or phenyl; and R3 is alkyl; and the preparation thereof by condensing a substituted 8-chloromethyl-7-methoxychromone in a solvent with a secondary amine in the molar ratio 1 : 2 under reflux boiling or in an autoclave, cooling and filtering the reaction mixture and concentrating it until dry under vacuum, taking up the residue in water and extracting the undissolved portion by means of a solvent, washing the extract with a saturated solution of sodium chloride and drying it over anhydrous sodium sulphate, mixing the washed and dried extract with an excess of alcoholic hydrochloric acid, concentrating it until dry under vacuum and recrystallising the residue from a solvent. Detailed examples are given. The compounds have a stimulating effect upon the central nervous system.
GB31111/59A 1958-09-12 1959-09-11 Chromones and processes for the preparation thereof Expired GB882537A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH882537X 1958-09-12

Publications (1)

Publication Number Publication Date
GB882537A true GB882537A (en) 1961-11-15

Family

ID=4544957

Family Applications (1)

Application Number Title Priority Date Filing Date
GB31111/59A Expired GB882537A (en) 1958-09-12 1959-09-11 Chromones and processes for the preparation thereof

Country Status (1)

Country Link
GB (1) GB882537A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0137193A2 (en) * 1983-08-12 1985-04-17 Hoechst Aktiengesellschaft Chromane alkaloid, process for its isolation from Dysoxylum binectariferum, and its use as a medicament
CN110240585A (en) * 2019-06-10 2019-09-17 上海诗丹德标准技术服务有限公司 A kind of preparation method of agalloch eaglewood tetrol

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0137193A2 (en) * 1983-08-12 1985-04-17 Hoechst Aktiengesellschaft Chromane alkaloid, process for its isolation from Dysoxylum binectariferum, and its use as a medicament
EP0137193A3 (en) * 1983-08-12 1987-02-04 Hoechst Aktiengesellschaft Chromane alkaloid, process for its isolation from dysoxylum binectariferum, and its use as a medicament
CN110240585A (en) * 2019-06-10 2019-09-17 上海诗丹德标准技术服务有限公司 A kind of preparation method of agalloch eaglewood tetrol
CN110240585B (en) * 2019-06-10 2023-08-22 上海诗丹德标准技术服务有限公司 Preparation method of agilawood tetraol

Similar Documents

Publication Publication Date Title
Weisblat et al. The Cleavage of Sulfonamides1
Lewin et al. 1, 5-hydrogen transfer during diazonium ion decomposition—IV: The copper catalyzed reaction. A Case of hydrogen atom or hydride ion transfer in the same system
SU417936A3 (en)
GB882537A (en) Chromones and processes for the preparation thereof
Veer et al. Note on the reaction between pyridine and benzyl magnesium chloride
GB1055184A (en) A process for the manufacture of 2-styryl-oxazole compounds
GB852604A (en) New anthraquinone dyestuffs
Paquette Dihydroazepinone Chemistry. III. The Base-Catalyzed Deuterium Exchange of 1, 3-Dihydro-1, 3, 5, 7-tetramethyl-2H-azepin-2-one1
SU72463A2 (en) Method for producing apomorphine
SU126227A1 (en) Method of isomerization of 3-methyl-3-ol-4-in-penta-en 1 to 3-methylpent-en-2-yn-4-ol-1 using ion exchange resins
SU70499A1 (en) The method of producing sulfanylguanidine
SU133872A1 (en) The method of obtaining the Quaternary ammonium salts
GB899386A (en) d-2-phenyl-3-methyltetrahydro-1,4-oxazine and a method of manufacturing same
SU129814A1 (en) The method of obtaining diphenylolpropane
SU398547A1 (en) METHOD OF OBTAINING DERIVATIVES OF 5H, 2,3,6,7-TETRAHYDROIMIDAZO
GB1062877A (en) Improvements in and relating to the preparation of substituted carbinols
GB998525A (en) Process for the preparation of aldehydes and ketones
SU126885A1 (en) The method of obtaining the sodium salt of 8-mercaptoquinoline (thioxin)
Cook et al. Isolation of acetic acid from mammalian liver
Grinev et al. Synthesis of alkylamine derivatives of 1-aryl-5-hydroxyindole
JPS5547652A (en) Production of substituted sulfondiimine
GB847016A (en) Improvements in or relating to a process for the preparation of and compositions comprising methyl mercuric nitrile
GB982572A (en) Improvements in and relating to quaternary ammonium compounds and the preparation thereof
GR27795B (en) METHOD FOR THE PREPARATION OF NEW HETEROCYCLIC COMPOUNDS.
ES270975A3 (en) Procedure for obtaining a mixture of polybromed salicilanylides (Machine-translation by Google Translate, not legally binding)