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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 604867생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/604867

반응식

참여 물질

역할이름HCID투입량
반응물[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]thioureaHCID 71650841—
반응물2-Chloro-1-(3-chloro-phenyl)-pentan-3-oneHCID 86624671—
생성물[5-(3-Chloro-benzyl)-4-ethyl-thiazol-2-yl]-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amineHCID 86624672—

반응 단계

The title compound was prepared in analogy to example 1 step e) from 76 mg (0.33 mmol) 2-chloro-1-(3-chloro-phenyl)-pentan-3-one and 79 mg (0.3 mmol) [3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-thiourea. The crude product was purified on silica gel with methylene chloride/methanol 19/1 yielding 62 mg (47%) [5-(4-chloro-benzyl)-4-ethyl-thiazol-2-yl]-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amine as a light brown viscous oil. MS ISP (m/e): 439.2/441.2 (100/40) (M+H)+. 1H NMR (DMSO-D6, 250 MHz): δ (ppm)=10.19 (s, 1H), 7.74 (s, 1H), 7.64 (s, 1H), 7.35-7.18 (m, 5H), 7.10 (d, 1H), 7.02 (s, 1H), 4.02 (s, 2H), 3.79 (s, 3H), 2.56 (q, 2H), 2.14 (s, 3H), 1.20 (t, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07910740B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-0daf4cab85f94ca99697acfc94355a20
출처 메모uspto-grants-2011_03