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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604881Generated: October 30, 2026

2-bromo-1-(5-bromo-2-methoxyphenyl)ethanone → HCID 25107258, compound

https://huagongshe.com/reaction/604881

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-bromo-1-(5-bromo-2-methoxyphenyl)ethanoneHCID 2756850—
Reactant[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]thioureaHCID 71650841—
SolventDiethyl EtherHCID 3283—
ProductHCID 25107258HCID 25107258104%

Reaction Steps

The title compound was prepared in analogy to example 1 step e) from 102 mg (0.33 mmol) 2-bromo-1-(5-bromo-2-methoxyphenyl)ethanone and 79 mg (0.3 mmol) [3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-thiourea. The crude reaction was diluted with diethyl ether and stirred for 15 minutes at room temperature. The product was filtered off and dried to yield 147 mg (99%) [4-(5-bromo-2-methoxy-phenyl)-thiazol-2-yl]-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amine as a white solid. MS ISP (m/e): 472.8/470.9 (100/93) (M+H)+. 1H NMR (DMSO-D6, 250 MHz): δ (ppm)=10.74 (s, 1H), 9.30 (s, 1H), 8.34 (dd, 1H), 7.70 (s, 1H), 7.60 (s, 1H), 7.51 (d, 1H), 7.47 (d, 1H), 7.13 (d, 1H), 7.05 (d, 1H), 4.00 (s, 3H), 3.95 (s, 3H), 2.35 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910740B2
Source datasetuspto-grants-2011_03
ORD IDord-87a73dcdbfe840f1898c3d87b681a1ee
Source noteuspto-grants-2011_03