GB1200892A - Production of 2-aminomethyl-2,3-dihydrobenzofurans - Google Patents
Production of 2-aminomethyl-2,3-dihydrobenzofuransInfo
- Publication number
- GB1200892A GB1200892A GB4832566A GB4832566A GB1200892A GB 1200892 A GB1200892 A GB 1200892A GB 4832566 A GB4832566 A GB 4832566A GB 4832566 A GB4832566 A GB 4832566A GB 1200892 A GB1200892 A GB 1200892A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dihydrobenzofurans
- aminomethyl
- oct
- compounds
- production
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- C07D307/81—Radicals substituted by nitrogen atoms not forming part of a nitro radical
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
1,200,892. 2 - Aminomethyl - 2,3 - dihydrobenzofurans. WARD BLENKINSOP & CO. 24 Oct., 1967 [27 Oct., 1966], No. 48325/66. Heading C2C. Compounds of formula wherein R, R<SP>1</SP> are each H, halogen or C 1-6 alkyl or alkoxy, are prepared by (a) heating the corresponding phthalimidomethyldihydrobenzofuran with hydrazine in a mutual solvent therefor, or (b) catalytically reducing the corresponding benzylaminomethyldihydrobenzofuran; the products may be converted to their acid addition salts. Compounds of the above formula wherein (a) R<SP>1</SP> is H and R is 5-Me, 5-MeO or 5-Cl, and (b) R, R 1 are 4,6-Me 2 , and their hydrochlorides, are claimed per se.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4832566A GB1200892A (en) | 1966-10-27 | 1966-10-27 | Production of 2-aminomethyl-2,3-dihydrobenzofurans |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4832566A GB1200892A (en) | 1966-10-27 | 1966-10-27 | Production of 2-aminomethyl-2,3-dihydrobenzofurans |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1200892A true GB1200892A (en) | 1970-08-05 |
Family
ID=10448205
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4832566A Expired GB1200892A (en) | 1966-10-27 | 1966-10-27 | Production of 2-aminomethyl-2,3-dihydrobenzofurans |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1200892A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4500543A (en) * | 1982-06-01 | 1985-02-19 | Abbott Laboratories | Substituted 1-aminomethyl-phthalans |
US7435837B2 (en) | 2003-10-24 | 2008-10-14 | Wyeth | Dihydrobenzofuranyl alkanamine derivatives and methods for using same |
US7728155B2 (en) | 2003-10-24 | 2010-06-01 | Wyeth Llc | Dihydrobenzofuranyl alkanamines and methods for using same as cns agents |
-
1966
- 1966-10-27 GB GB4832566A patent/GB1200892A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4500543A (en) * | 1982-06-01 | 1985-02-19 | Abbott Laboratories | Substituted 1-aminomethyl-phthalans |
US7435837B2 (en) | 2003-10-24 | 2008-10-14 | Wyeth | Dihydrobenzofuranyl alkanamine derivatives and methods for using same |
US7728155B2 (en) | 2003-10-24 | 2010-06-01 | Wyeth Llc | Dihydrobenzofuranyl alkanamines and methods for using same as cns agents |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |