CN106146289A - The synthetic method of medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt - Google Patents

The synthetic method of medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt Download PDF

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Publication number
CN106146289A
CN106146289A CN201510761467.2A CN201510761467A CN106146289A CN 106146289 A CN106146289 A CN 106146289A CN 201510761467 A CN201510761467 A CN 201510761467A CN 106146289 A CN106146289 A CN 106146289A
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China
Prior art keywords
carboxylic acid
acid salt
synthetic method
oxo
medicine intermediate
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Pending
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CN201510761467.2A
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Chinese (zh)
Inventor
彭海燕
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.)
WUXI QIANHAO BIO-PHARMACEUTICAL Co Ltd
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WUXI QIANHAO BIO-PHARMACEUTICAL Co Ltd
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Priority to CN201510761467.2A priority Critical patent/CN106146289A/en
Publication of CN106146289A publication Critical patent/CN106146289A/en
Pending legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/347Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
    • C07C51/353Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by isomerisation; by change of size of the carbon skeleton

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

Abstract

The present invention relates to the synthetic method of a kind of medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt, with carboxylate as raw material, under solvent methanol effect, first react with oxo ring fourth at temperature 120 DEG C-150 DEG C, then generate 4-oxo cyclobutane yl carboxylic acid salt by alkylation.The synthetic method of medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt of the present invention is simple, efficient, and operates safety, very useful in concrete production.

Description

The synthetic method of medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt
Technical field
The present invention relates to the synthetic method of a kind of medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt.
Background technology
4-oxo cyclobutane yl carboxylic acid salt is the initiation material of many pharmaceutical synthesis, the important intermediate of particularly a lot of carboxylate compounds, the domestic at present synthetic method having no this compound of report.
Content of the invention
It is an object of the invention to overcome above-mentioned deficiency, provide a kind of simple, efficiently, the synthetic method of the medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt of safety operation.
The object of the present invention is achieved like this:
The synthetic method of a kind of medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt, with carboxylate as raw material, under solvent methanol effect, first reacts with oxo ring fourth at temperature 120 DEG C-150 DEG C, then generates 4-oxo cyclobutane yl carboxylic acid salt by alkylation.
Compared with prior art, the invention has the beneficial effects as follows:
The synthetic method of medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt of the present invention is simple, efficient, and operates safety, very useful in concrete production.
Detailed description of the invention
The synthetic method of medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt of the present invention is specific as follows:
With carboxylate as raw material, under solvent methanol effect, first react with oxo ring fourth at temperature 120 DEG C-150 DEG C, then generate 4-oxo cyclobutane yl carboxylic acid salt by alkylation.The purity of this crude product can meet general reaction requirement, can direct plunge in reaction.

Claims (1)

1. the synthetic method of a medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt, it is characterized in that with carboxylate as raw material, under solvent methanol effect, first react with oxo ring fourth at temperature 120 DEG C-150 DEG C, then generate 4-oxo cyclobutane yl carboxylic acid salt by alkylation.
CN201510761467.2A 2015-11-11 2015-11-11 The synthetic method of medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt Pending CN106146289A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510761467.2A CN106146289A (en) 2015-11-11 2015-11-11 The synthetic method of medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510761467.2A CN106146289A (en) 2015-11-11 2015-11-11 The synthetic method of medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt

Publications (1)

Publication Number Publication Date
CN106146289A true CN106146289A (en) 2016-11-23

Family

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CN201510761467.2A Pending CN106146289A (en) 2015-11-11 2015-11-11 The synthetic method of medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt

Country Status (1)

Country Link
CN (1) CN106146289A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109206311A (en) * 2018-10-26 2019-01-15 山东谛爱生物技术有限公司 A kind of preparation method of 3- oxo cyclobutane yl carboxylic acid

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109206311A (en) * 2018-10-26 2019-01-15 山东谛爱生物技术有限公司 A kind of preparation method of 3- oxo cyclobutane yl carboxylic acid

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PB01 Publication
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WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20161123