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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2075975생성일: 2026년 10월 26일

4-(1,2,4-Triazol-1-yl)phenylthiourea → (4-Phenyl-4,5,6,7-tetrahydro-benzothiazol-2-yl)-(4-[1,2,4]triazol-1-yl-phenyl)-amine

https://huagongshe.com/reaction/2075975

반응식

참여 물질

역할이름HCID투입량
반응물4-(1,2,4-Triazol-1-yl)phenylthioureaHCID 5260678—
반응물2-Bromo-6-phenylcyclohexanoneHCID 12779129—
용매EthanolHCID 702—
생성물(4-Phenyl-4,5,6,7-tetrahydro-benzothiazol-2-yl)-(4-[1,2,4]triazol-1-yl-phenyl)-amineHCID 5739911964.3%

반응 단계

A suspension of 4-(1,2,4-triazol-1-yl)phenylthiourea (109.6 mg, 0.5 mmol) and of 2-bromo-6-phenyl-cyclohexanone (253.1 mg, 1.00 mmol) in ethanol (4 mL) was heated for two days to reflux under an atmosphere of nitrogen. After cooling to room temperature the solvent was evaporated under reduced pressure and the residue was treated with dichloromethane, diethyl ether and heptane. The product precipitated as a solid and was filtered off to yield the title compound (120 mg, 64%) as a pale-brown solid. MS ISP (m/e): 374.3 (100) [(M+H)+]. 1H NMR (DMSO-D6, 300 MHz): δ (ppm)=10.4 (s, 1H), 9.38 (s, 1H), 8.29 (s, 1H), 8.02 (d, 2H), 7.56 (d, 2H), 7.30 (t, 2H), 7.10-7.19 (m, 5H), 4.00 (m, 1H), 2.72 (m, 2H), 2.14 (m, 1.70-1.89 (m, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07923450B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-b010277627c24eb3b246654ff4874675
출처 메모uspto-grants-2011_04