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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1803260생성일: 2026년 10월 26일

2-Bromo-6-phenylcyclohexanone → N-(3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl)-4-phenyl-4,5,6,7-tetrahydrobenzo[d]thiazol-2-amine

https://huagongshe.com/reaction/1803260

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-6-phenylcyclohexanoneHCID 12779129—
반응물1-(3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl)thioureaHCID 86649898—
용매EthanolHCID 702—
용매Ethyl AcetateHCID 8857—
생성물N-(3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl)-4-phenyl-4,5,6,7-tetrahydrobenzo[d]thiazol-2-amineHCID 4686432239%

반응 단계

A mixture of 2-bromo-6-phenylcyclohexanone (84 mg, 0.332 mmol, from preparation AAA) and 1-(3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl)thiourea (87 mg, 0.332 mmol, from step 4 of preparation F) was heated in ethanol (0.55 mL) at 80° C. for 3 h. The crude reaction was diluted with EtOAc and washed with saturated sodium bicarbonate solution. The organic layer was concentrated in vacuo. The crude product was purified using preparatory TLC (60% acetone/hexanes) to give 54 mg (39% yield) of the titled compound as a white solid. LC-MS (M+H)+ 418.0. 1H NMR (400 MHz, chloroform-d) δ ppm 8.44 (s, 1 H) 7.49 (dd, J=5.41, 3.15 Hz, 2 H) 7.23-7.35 (m, 2 H) 7.12-7.21 (m, 3 H) 6.60 (dd, J=8.56, 2.27 Hz, 1H) 3.98-4.08 (m, 1 H) 3.49 (s, 3 H) 2.66-2.85 (m, 2 H) 2.46 (s, 3 H) 2.17-2.26 (m, 1 H) 1.92-2.05 (m, 1 H) 1.78-1.91 (m, 2 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08349880B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-75451273d3b04d6aa1661d0c9f4735ea
출처 메모uspto-grants-2013_01