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HRID 2075974作成日:2026年10月25日

2-Bromo-6-phenylcyclohexanone → (3-Methoxy-4-oxazol-5-yl-phenyl)-(4-phenyl-4,5,6,7-tetrahydro-benzothiazol-2-yl)-amine

https://huagongshe.com/reaction/2075974

反応式

関与物質

役割名称HCID仕込み量
反応物2-Bromo-6-phenylcyclohexanoneHCID 12779129—
反応物(3-Methoxy-4-oxazol-5-yl-phenyl)-thioureaHCID 22459682—
溶媒EthanolHCID 702—
生成物(3-Methoxy-4-oxazol-5-yl-phenyl)-(4-phenyl-4,5,6,7-tetrahydro-benzothiazol-2-yl)-amineHCID 5778072683.4%

反応手順

A suspension of (3-methoxy-4-oxazol-5-yl-phenyl)-thiourea (74.8 mg, 0.3 mmol) and of 2-bromo-6-phenyl-cyclohexanone (75.9 mg, 0.3 mmol, preparation: WO9404487) in ethanol (4 mL) was heated over night to reflux under an atmosphere of nitrogen. After cooling to room temperature the solvent was evaporated under reduced pressure and the residue was purified on silica gel using dichloromethane/methanol (19:1 v/v) as eluent to yield the title compound (101 mg, 83%) as an off-white foam. MS ISP (m/e): 404.5 (100) [(M+H)+]. 1H NMR (DMSO-D6, 300 MHz): δ (ppm)=10.29 (s, 1H), 8.31 (s, 1H), 7.66 (s, 1H), 7.50 (d, 1H), 7.46-7.51 (m, 3H), 7.09-7.31 (m, 3H), 6.83 (s, 1H), 4.00 (m, 1H), 3.46 (s, 3H), 2.73 (m, 2H), 2.12 (m, 1H), 1.70-1.94 (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-f7d6574307724d029c3157fc7e6614fe
出典メモuspto-grants-2011_04