GB765853A - Improvements in or relating to substituted piperidines - Google Patents
Improvements in or relating to substituted piperidinesInfo
- Publication number
- GB765853A GB765853A GB9091/53A GB909153A GB765853A GB 765853 A GB765853 A GB 765853A GB 9091/53 A GB9091/53 A GB 9091/53A GB 909153 A GB909153 A GB 909153A GB 765853 A GB765853 A GB 765853A
- Authority
- GB
- United Kingdom
- Prior art keywords
- product
- methyl
- diphenyl
- phenyl
- pyridyl
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
The invention comprises vinylpiperidine compounds of the general formula <FORM:0765853/IV(b)/1> (wherein Q is phenyl, Q1 is phenyl or pyridyl and R2 is hydrogen or an alkyl group of 1-6 carbon atoms) and their acid addition and quaternary ammonium salts, and the manufacture thereof by dehydrating a carbinol of the general formula: <FORM:0765853/IV(b)/2> (wherein one of R and R1 is hydrogen and the other a hydroxy group), followed, if desired and necessary, by reductive alkylation of the product, and further, if desired, by conversion of the product into an acid addition or quaternary ammonium salt thereof. In examples: (1)-(3) diphenyl 4-, 3- and 2-pipecolyl carbinols are heated with 85 per cent sulphuric acid to produce 4 -, 3 - and 2 - (b : b - diphenyl)-vinylpiperidine, isolated in the form of their hydrochlorides; (4) diphenyl 1-methyl-2-pipecolyl carbinol oxalate similarly yields 2-(b : b -diphenyl) - vinyl - 1 - methylpiperidine hydrochloride; (5) a -(2-pyridyl)-benzyl 1-methyl-4-piperidyl carbinol similarly gives 4-[b -(2-pyridyl)-b - phenyl] - vinyl - 1 - methylpiperidine hydrochloride; (6) the product of (1) is warmed with formalin and formic acid, followed by treatment with caustic potash to liberate 4-(b : b - diphenyl) - vinyl - 1 - methylpiperidine; (7) the product of (6) is quaternated with methyl bromide; (8) the product of (3) is methylated as in (6) to form the same product as in (4); (9) and (10) the product of (4) or (8) is quaternated with methyl bromide and with methyl iodide. The products, especially in the form of salts (e.g. sulphates, phosphate, hydrochlorides, levulinates, mucates, acetates and tartrates) are useful as antispasmodic agents. Additional quaternizing reagents specified are ethyl chloride, methyl sulphate, methyl p-toluenesulphonate and benzyl bromide. Specification 765,854 is referred to.ALSO:Therapeutic preparations for the relief of smooth-muscle spasms contain vinylpiperidine compounds of the general formula:- <FORM:0765853/VI/1> (wherein Q is phenyl, Q1 is phenyl or pyridyl and R2 is hydrogen or an alkyl group of 1-6 carbon atoms) or an acid addition or quaternary ammonium salt thereof. These compounds may be employed in the form of an aqueous solution of a water-soluble salt (e.g. of sulphuric, phosphoric, hydrochloric, leonlinic, mucic, acetic or tartaric acid) or incorporated in a tablet or capsule base. The free bases or their sparingly soluble salts may be administered when a slow and prolonged effect is desired. The quaternary ammonium salts (e.g. methobromides and methiodides) have a particularly powerful action. Specification 765,854 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US765853XA | 1952-04-03 | 1952-04-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB765853A true GB765853A (en) | 1957-01-16 |
Family
ID=22132962
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB9091/53A Expired GB765853A (en) | 1952-04-03 | 1953-04-01 | Improvements in or relating to substituted piperidines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB765853A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008508307A (en) * | 2004-07-29 | 2008-03-21 | メルク エンド カムパニー インコーポレーテッド | Potassium channel inhibitor |
CN110981787A (en) * | 2018-12-27 | 2020-04-10 | 泰州医药城国科化物生物医药科技有限公司 | 2- (2, 2-diaryl vinyl) -quaternary ammonium salt type cyclic amine derivative and preparation method thereof |
-
1953
- 1953-04-01 GB GB9091/53A patent/GB765853A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008508307A (en) * | 2004-07-29 | 2008-03-21 | メルク エンド カムパニー インコーポレーテッド | Potassium channel inhibitor |
US7879839B2 (en) | 2004-07-29 | 2011-02-01 | Merck Sharp & Dohme Corp. | Potassium channel inhibitors |
JP4719745B2 (en) * | 2004-07-29 | 2011-07-06 | メルク・シャープ・エンド・ドーム・コーポレイション | Potassium channel inhibitor |
CN110981787A (en) * | 2018-12-27 | 2020-04-10 | 泰州医药城国科化物生物医药科技有限公司 | 2- (2, 2-diaryl vinyl) -quaternary ammonium salt type cyclic amine derivative and preparation method thereof |
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