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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 604889생성일: 2026년 10월 25일

2-Chlorocyclopentanone → (5,6-Dihydro-4H-cyclopentathiazol-2-yl)-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amine

https://huagongshe.com/reaction/604889

반응식

참여 물질

역할이름HCID투입량
반응물2-ChlorocyclopentanoneHCID 12751—
반응물[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]thioureaHCID 71650841—
용매EthanolHCID 702—
용매1,4-DioxaneHCID 31275—
생성물(5,6-Dihydro-4H-cyclopentathiazol-2-yl)-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amineHCID 86624684—

반응 단계

The title compound was prepared in analogy to example 1 step e) from 40 mg (0.33 mmol) 2-chlorocyclopentanone and 79 mg (0.3 mmol) [3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-thiourea in ethanol (1.5 ml) and dioxane (1.5 ml). The crude product was purified on silica gel with methylene chloride/methanol 19/1 yielding 41 mg (42%) (5,6-dihydro-4H-cyclopentathiazol-2-yl)-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amine as a light yellow solid. MS ISP (m/e): 327.3 (100) (M+H)+. 1H NMR (DMSO-D6, 250 MHz): δ (ppm)=10.25 (s, 1H), 7.64 (s, 1H), 7.44 (s, 1H), 7.32 (d, 1H), 7.23 (d, 1H), 7.01 (s, 1H), 3.78 (s, 3H), 2.78 (br t, 2H), 2.67 (br t, 2H), 2.35 (m, 2H), 2.14 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07910740B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-cc5873822b76497ba47a64eb0645e7a6
출처 메모uspto-grants-2011_03