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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076133Generated: October 31, 2026

2-Bromo-6-phenylcyclohexanone → [4-(2,4-Dimethyl-thiazol-5-yl)-3-methoxy-phenyl]-(4-phenyl-4,5,6,7-tetrahydro-benzothiazol-2-yl)-amine

https://huagongshe.com/reaction/2076133

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-6-phenylcyclohexanoneHCID 12779129—
Reactant[4-(2,4-Dimethyl-thiazol-5-yl)-3-methoxy-phenyl]-thioureaHCID 86632613—
SolventEthanolHCID 702—
Product[4-(2,4-Dimethyl-thiazol-5-yl)-3-methoxy-phenyl]-(4-phenyl-4,5,6,7-tetrahydro-benzothiazol-2-yl)-amineHCID 44193960100%

Reaction Steps

A solution of [4-(2,4-dimethyl-thiazol-5-yl)-3-methoxy-phenyl]-thiourea (88 mg, 0.30 mmol) and 2-bromo-6-phenyl-cyclohexanone (80 mg, 0.32 mmol) in ethanol (3 ml) was heated to reflux over night. The precipitated solid was filtered off after cooling to room temperature and dried to yield the title compound (100 mg, 100%) as a yellow solid. MS ISP (m/e): 448.2 (100) [(M+H)+]. 1H NMR (DMSO-D6, 300 MHz): δ (ppm)=10.27 (br s, 1H, NH), 7.59 (s, 1H), 7.28 (t, 2H), 7.12-7.19 (m, 4H), 6.85 (d, 1H), 4.00 (m, 1H), 3.37 (s, 3H), 2.74 (m, 2H), 2.66 (s, 3H), 2.20 (s, 2H), 2.13 (m, 1H), 1.70-1.93 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923450B2
Source datasetuspto-grants-2011_04
ORD IDord-d04d7e206a2040e7a43548a31c314d87
Source noteuspto-grants-2011_04