FR1057372A - basic ethers and their preparation - Google Patents

basic ethers and their preparation

Info

Publication number
FR1057372A
FR1057372A FR1057372DA FR1057372A FR 1057372 A FR1057372 A FR 1057372A FR 1057372D A FR1057372D A FR 1057372DA FR 1057372 A FR1057372 A FR 1057372A
Authority
FR
France
Prior art keywords
preparation
basic ethers
ethers
basic
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
Other languages
French (fr)
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.)
Hoechst AG
Original Assignee
Hoechst AG
Farbwerke Hoechst AG
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 Hoechst AG, Farbwerke Hoechst AG filed Critical Hoechst AG
Application granted granted Critical
Publication of FR1057372A publication Critical patent/FR1057372A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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
    • C07D211/40Oxygen atoms
    • C07D211/44Oxygen atoms attached in position 4
FR1057372D 1951-05-26 1952-05-26 basic ethers and their preparation Expired FR1057372A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE1057372X 1951-05-26

Publications (1)

Publication Number Publication Date
FR1057372A true FR1057372A (en) 1954-03-08

Family

ID=7718107

Family Applications (1)

Application Number Title Priority Date Filing Date
FR1057372D Expired FR1057372A (en) 1951-05-26 1952-05-26 basic ethers and their preparation

Country Status (1)

Country Link
FR (1) FR1057372A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0364941A1 (en) * 1988-10-21 1990-04-25 Hoechst Aktiengesellschaft Branched-chain alkyl esters of 2-(4-(2-piperidino ethoxy)benzoyl)benzoic acid, processes for their preparation and their use as spasmolytic agents
US5821252A (en) * 1988-10-21 1998-10-13 Hoechst Aktiengesellschaft Method of blocking nerve conduction by treatment with branched-chain esters of 2- 4-(2-piperidine-ethoxy)-benzoyl!-benzoic acid and pharmaceutically acceptable salts thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0364941A1 (en) * 1988-10-21 1990-04-25 Hoechst Aktiengesellschaft Branched-chain alkyl esters of 2-(4-(2-piperidino ethoxy)benzoyl)benzoic acid, processes for their preparation and their use as spasmolytic agents
US5821252A (en) * 1988-10-21 1998-10-13 Hoechst Aktiengesellschaft Method of blocking nerve conduction by treatment with branched-chain esters of 2- 4-(2-piperidine-ethoxy)-benzoyl!-benzoic acid and pharmaceutically acceptable salts thereof

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