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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 280676생성일: 2026년 10월 25일

Acetic Acid → 5-Amino-1-(3-chloro-4-[4-chlorobenzoyl]-5-methylbenzyl)-1,2,3-triazole-4-carboxamide

https://huagongshe.com/reaction/280676

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물CyanoacetamideHCID 7898—
반응물SodiumHCID 5360545—
반응물3-Chloro-4-(4-chlorobenzoyl)-5-methylbenzyl azideHCID 23320962—
용매EthanolHCID 702—
생성물5-Amino-1-(3-chloro-4-[4-chlorobenzoyl]-5-methylbenzyl)-1,2,3-triazole-4-carboxamideHCID 1364967567.3%

반응 단계

A stirred, 60° C. solution of sodium (88.7 mg, 3.84 mmol) in absolute ethanol (9.6 ml) was treated with 2-cyanoacetamide (323 mg, 3.84 mmol), kept 5 min., and treated with 3-chloro-4-(4-chlorobenzoyl)-5-methylbenzyl azide (1.03 g, 3.20 mmol). The mixture was refluxed 1 hour, cooled to ambient temperature, acidified with glacial acetic acid (487 μl, 511 mg, 7.68 mmol), and evaporated to dryness at 30° C. under vacuum. The residue was chromatographed on a column of silica gel (150 g) eluted in 17 ml fractions with 19:1 (v/v) dichloromethane-methanol. Fractions 22-38 were combined and evaporated to dryness. The residual glass was kept 18 hours at ambient temperature with diethyl ether (25 ml), filtered, washed with diethyl ether, and dried to provide 870 mg (67%) crystalline 5-amino-1-(3-chloro-4-[4-chlorobenzoyl]-5-methylbenzyl)-1,2,3-triazole-4 -carboxamide, m.p. 205°-206° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04590201
출처 데이터셋uspto-grants-1986_05
ORD IDord-9b62d756e4a44b1ab9e811dfda3503a7
출처 메모uspto-grants-1986_05