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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076129Generated: October 30, 2026

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

https://huagongshe.com/reaction/2076129

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-6-phenylcyclohexanoneHCID 12779129—
Reactant[3-Methoxy-4-(2-methyl-thiazol-5-yl)-phenyl]-thioureaHCID 86632612—
SolventEthanolHCID 702—
Product[3-Methoxy-4-(2-methyl-thiazol-5-yl)-phenyl]-(4-phenyl-4,5,6,7-tetrahydro-benzothiazol-2-yl)-amineHCID 4419386094.6%

Reaction Steps

A solution of [3-methoxy-4-(2-methyl-thiazol-5-yl)-phenyl]-thiourea (110 mg, 0.39 mmol) and 2-bromo-6-phenyl-cyclohexanone (105 mg, 0.41 mmol) in ethanol (4 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 (160 mg, 94%) as a yellow solid. MS ISP (m/e): 434.3 (100) [(M+H)+]. 1H NMR (DMSO-D6, 300 MHz): δ (ppm)=10.32 (br s, 1H, NH), 8.10 (s, 1H), 7.61 (s, 1H), 7.56 (d, 1H), 7.29 (t, 2H), 7.15-7.21 (m, 3H), 6.85 (d, 1H), 4.00 (m, 1H), 3.48 (s, 3H), 2.75 (m, 2H), 2.68 (s, 3H), 2.14 (m, 1H), 1.70-1.94 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923450B2
Source datasetuspto-grants-2011_04
ORD IDord-7033ec88da9844b78e86bbcc5424bc2e
Source noteuspto-grants-2011_04