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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075993Generated: October 30, 2026

6-Bromo-2-(4-trifluoromethoxy-phenyl)-cyclohexanone → [3-Methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-[4-(4-trifluoromethoxy-phenyl)-4,5,6,7-tetrahydro-benzothiazol-2-yl]-amine

https://huagongshe.com/reaction/2075993

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-2-(4-trifluoromethoxy-phenyl)-cyclohexanoneHCID 67096134—
Reactant[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]thioureaHCID 71650841—
SolventEthanolHCID 702—
Product[3-Methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-[4-(4-trifluoromethoxy-phenyl)-4,5,6,7-tetrahydro-benzothiazol-2-yl]-amineHCID 4419508917.8%

Reaction Steps

A suspension of [3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-thiourea (48 mg, 0.18 mmol) and of crude 6-bromo-2-(4-trifluoromethoxyl-phenyl)-cyclohexanone (65 mg, 0.19 mmol) in ethanol (2 mL) was heated to reflux under an atmosphere of nitrogen for 2 days. After cooling to room temperature the solvent was evaporated under reduced pressure and the residue was purified by reversed preparative HPLC using acetonitril/water (0.1% formic acid) to yield the title compound (16 mg, 17%) as a pale-brown oil. MS ISP (m/e): 501.0 (100) [(M+H)+]. 1H NMR (CDCl3, 300 MHz): δ (ppm)=7.61 (s, 1H), 7.35 (s, 1H), 7.08-7.20 (m, 4H), 6.82 (s, 1H), 6.65 (d, 1H), 4.06 (m, 1H), 3.56 (s, 3H), 2.75 (m, 2H), 2.28 (s, 3H), 2.25 (m, 1H), 1.77-1.98 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923450B2
Source datasetuspto-grants-2011_04
ORD IDord-cc155bc24a9944c5b66259bd1ff41811
Source noteuspto-grants-2011_04