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HRID 1723442作成日:2026年10月25日

1-(4-Fluorobenzoyl)aziridine → N-[2-[4-[(2-benzoxazolyl)amino]-1-piperidinyl]ethyl]-4-fluorobenzamide

https://huagongshe.com/reaction/1723442

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-Fluorobenzoyl)aziridineHCID 84853—
反応物N-(4-piperidinyl)-2-benzoxazolamineHCID 14575294—
溶媒TolueneHCID 1140—
生成物N-[2-[4-[(2-benzoxazolyl)amino]-1-piperidinyl]ethyl]-4-fluorobenzamideHCID 1572519834%

反応手順

A mixture of 1.65 parts of 1-(4-fluorobenzoyl)aziridine (solution in benzene 1.2M), 2.1 parts of N-(4-piperidinyl)-2-benzoxazolamine and 90 parts of methylbenzene was stirred and refluxed overnight. The reaction mixture was evaporated and the residue was crystallized from 2-propanol. The product was filtered off and recrystallized from 2-propanone, yielding 1.3 parts (34%) of N-[2-[4-[(2-benzoxazolyl)amino]-1-piperidinyl]ethyl]-4-fluorobenzamide; mp. 173.3° C. (448).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04861785
出典データセットuspto-grants-1989_08
ORD IDord-c96379a3ad85495eb98b42ab4e1729d9
出典メモuspto-grants-1989_08