JPS5679671A - Preparation of imidazoles - Google Patents

Preparation of imidazoles

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Publication number
JPS5679671A
JPS5679671A JP15586579A JP15586579A JPS5679671A JP S5679671 A JPS5679671 A JP S5679671A JP 15586579 A JP15586579 A JP 15586579A JP 15586579 A JP15586579 A JP 15586579A JP S5679671 A JPS5679671 A JP S5679671A
Authority
JP
Japan
Prior art keywords
imidazoles
trifunctional
oxyacid ester
triarylmethylimidazoles
triarylmethanols
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.)
Pending
Application number
JP15586579A
Other languages
Japanese (ja)
Inventor
Hideo Yasukui
Kitaro Saji
Mitsuo Nakashita
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP15586579A priority Critical patent/JPS5679671A/en
Publication of JPS5679671A publication Critical patent/JPS5679671A/en
Pending legal-status Critical Current

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Abstract

PURPOSE: To obtain 1-triarylmethylimidazoles having antigungal activities, by reacting triarylmethanols with 1-unsubstituted-imidazoles in the presence of a trifunctional phosphorus oxyacid ester.
CONSTITUTION: Triarylmethanols triphenylmethanol is omitted shown by the formula (A, B, and D are aromatic heterocylic ring, or phenyl, with the proviso that one of A, B, and D is necessarily aromatic heterocyclic group) in reacted with 1- unsubstituted-imidazoles in the presence of a trifunctional phosphorus oxyacid ester in a solvent, e.g., methyl isobutyl ketone, etc. at 60W120°C to give 1-triarylmethylimidazoles (1-triphenylmethylimidazoles are omitted). An aryl phosphite, e.g., diphenyl phosphite, triphenyl phosphite, etc. is preferably used as the trifunctional oxyacid ester.
COPYRIGHT: (C)1981,JPO&Japio
JP15586579A 1979-11-30 1979-11-30 Preparation of imidazoles Pending JPS5679671A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15586579A JPS5679671A (en) 1979-11-30 1979-11-30 Preparation of imidazoles

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15586579A JPS5679671A (en) 1979-11-30 1979-11-30 Preparation of imidazoles

Publications (1)

Publication Number Publication Date
JPS5679671A true JPS5679671A (en) 1981-06-30

Family

ID=15615187

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15586579A Pending JPS5679671A (en) 1979-11-30 1979-11-30 Preparation of imidazoles

Country Status (1)

Country Link
JP (1) JPS5679671A (en)

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