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HRID 2075975作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物4-(1,2,4-Triazol-1-yl)phenylthioureaHCID 5260678—
反応物2-Bromo-6-phenylcyclohexanoneHCID 12779129—
溶媒EthanolHCID 702—
生成物(4-Phenyl-4,5,6,7-tetrahydro-benzothiazol-2-yl)-(4-[1,2,4]triazol-1-yl-phenyl)-amineHCID 5739911964.3%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07923450B2
出典データセットuspto-grants-2011_04
ORD IDord-b010277627c24eb3b246654ff4874675
出典メモuspto-grants-2011_04