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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 604870생성일: 2026년 10월 26일

Phosgene → [5-(3-Chloro-benzyl)-4-methyl-thiazol-2-yl]-(4-[1,2,4]triazol-1-yl-phenyl)-amine

https://huagongshe.com/reaction/604870

반응식

참여 물질

역할이름HCID투입량
반응물PhosgeneHCID 6371—
반응물DiisopropylethylamineHCID 81531—
반응물3-Chloro-4-(3-chlorophenyl)-2-butanoneHCID 4250985—
반응물4-(1,2,4-Triazol-1-yl)phenylthioureaHCID 5260678—
용매EthanolHCID 702—
생성물[5-(3-Chloro-benzyl)-4-methyl-thiazol-2-yl]-(4-[1,2,4]triazol-1-yl-phenyl)-amineHCID 25106457—

반응 조건

온도170 °C

반응 단계

A suspension of 55 mg (0.25 mmol) 4-(1,2,4-triazol-1-yl)phenylthiourea, of 60 mg (0.28 mmol) 3-chloro-4-(3-chlorophenyl)-2-butanone and of 65 mg (0.5 mmol) N,N-diisopropyl ethyl amine in ethanol (2.5 ml) was refluxed over night. The same amount of chloro ketone was added and the reaction was heated to reflux over night. Again 1.1 equivalent of chloro ketone was added and the reaction was heated for 10 minutes in a microwave oven to 170° C. The solvent was evaporated and the residue was purified on silica gel with methylene chloride/methanol 19/1 yielding 27 mg (28%) [5-(3-chloro-benzyl)-4-methyl-thiazol-2-yl]-(4-[1,2,4]triazol-1-yl-phenyl)-amine as a yellow solid. MS ISP (m/e): 382.1 (100) (M+H)+. 1H NMR (CDCl3, 250 MHz): δ (ppm)=8.48 (s, 1H), 8.09 (s, 1H), 7.60 (d, 2H), 7.46 (d, 2H), 7.25-7.18 (m, 3H), 7.09 (d, 1H), 3.96 (s, 2H), 2.29 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07910740B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-a3be7135f3944c2087df2195ee7e0bd6
출처 메모uspto-grants-2011_03