ES384512A1 - A method for preparing an oxazolyl derivative. (Machine-translation by Google Translate, not legally binding) - Google Patents

A method for preparing an oxazolyl derivative. (Machine-translation by Google Translate, not legally binding)

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Publication number
ES384512A1
ES384512A1 ES384512A ES384512A ES384512A1 ES 384512 A1 ES384512 A1 ES 384512A1 ES 384512 A ES384512 A ES 384512A ES 384512 A ES384512 A ES 384512A ES 384512 A1 ES384512 A1 ES 384512A1
Authority
ES
Spain
Prior art keywords
formula
group
see formula
see
oxazolyl
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
ES384512A
Other languages
Spanish (es)
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
Publication of ES384512A1 publication Critical patent/ES384512A1/en
Expired legal-status Critical Current

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  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

A method of preparing an oxazolyl derivative having the formula **(See formula)** wherein R1 and R2 each represent a hydrogen atom, an alcohol, cycloalkoxy, or aryl group which may be substituted by alcohol or alkoxy groups or halogen atoms, or R1 and R2 may be linked together to form a cycloalcohyl group and they can be the same or different; B represents a bivalent group; and X represents an oxazolyl group having the formula (II) **(See formula)** where R1 and R2 are the same as identified above, an aryloxazolyl group having the formula (III) **(See formula)** where A represents a benzene or naphthalene nucleus that may be substituted by alcohol groups or halogen atoms or when the bivalent group represented by B is **(See formula)** X represents the oxazolyl group having the formula (II), the aryloxazolyl group having the formula (III), or an aryl group having the formula (IV) **(See formula)** where R3 represents hydrogen or a halogen atom, an alkoxy, cyano, hydroxycarbonyl, alkoxycarbonyl, phenoxycarbonyl group, (see formula) or - NHC0R6 in which each of R4 and R5 represents a hydrogen atom or an alcoholic group and R6 represents an alcoholic or phenyl group, characterized in that it comprises reacting an alpha-aminoketone having the formula **(See formula)** wherein R1 and R2 are as defined above, with an acid halide having the formula **(See formula)** where B and X are as defined above and Hal means a halogen atom, in the presence of a base, and ring-closing the resulting acid amide having the formula **(See formula)** wherein R1, R2, B and X are as defined above in the presence of a dehydrating agent. (Machine-translation by Google Translate, not legally binding)
ES384512A 1969-10-21 1970-10-14 A method for preparing an oxazolyl derivative. (Machine-translation by Google Translate, not legally binding) Expired ES384512A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP8399069 1969-10-21
JP8746269 1969-10-30
JP8746169 1969-10-30

Publications (1)

Publication Number Publication Date
ES384512A1 true ES384512A1 (en) 1973-05-01

Family

ID=27304394

Family Applications (1)

Application Number Title Priority Date Filing Date
ES384512A Expired ES384512A1 (en) 1969-10-21 1970-10-14 A method for preparing an oxazolyl derivative. (Machine-translation by Google Translate, not legally binding)

Country Status (1)

Country Link
ES (1) ES384512A1 (en)

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