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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 604864생성일: 2026년 10월 25일

3-Chloro-4-(3-chlorophenyl)-2-butanone → [5-(3-Chloro-benzyl)-4-methyl-thiazol-2-yl]-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amine

https://huagongshe.com/reaction/604864

반응식

참여 물질

역할이름HCID투입량
반응물3-Chloro-4-(3-chlorophenyl)-2-butanoneHCID 4250985—
반응물[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]thioureaHCID 71650841—
용매EthanolHCID 702—
생성물[5-(3-Chloro-benzyl)-4-methyl-thiazol-2-yl]-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amineHCID 25052759—

반응 단계

A suspension of 78.7 mg (0.3 mmol) [3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-thiourea and of 71.6 mg (0.33 mmol) of 3-chloro-4-(3-chlorophenyl)-2-butanone in ethanol (3 ml) was heated over night to reflux to yield a yellow solution. After cooling to room temperature the solvent was evaporated under reduced pressure and the residue was purified on silica gel with methylene chloride/methanol 19/1 yielding 55 mg (43%) [5-(3-chloro-benzyl)-4-methyl-thiazol-2-yl]-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amine as a yellow solid. MS ISP (m/e): 425.1/427.2 (100/43) (M+H)+. 1H NMR (DMSO-D6, 250 MHz): δ (ppm)=10.16 (s, 1H), 7.64 (s, 1H), 7.53 (s, 1H), 7.35-7.19 (m, 6H), 7.01 (s, 1H), 4.01 (s, 2H), 3.78 (s, 3H), 2.24 (s, 3H), 2.14 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07910740B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-b04ff111fd5040e787dc9c53c13234b4
출처 메모uspto-grants-2011_03