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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243076Generated: October 31, 2026

Phenacyl bromide → 1-(5-Bromo-4-(4-phenylthiazol-2-yl)pyridin-2-yl)-3-ethylurea

https://huagongshe.com/reaction/2243076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantAZD7118 Bromo ThioamideHCID 59208439—
SolventAcetonitrileHCID 6342—
Product1-(5-Bromo-4-(4-phenylthiazol-2-yl)pyridin-2-yl)-3-ethylureaHCID 5920850484.7%

Reaction Steps

To a mixture of 5-bromo-2-(3-ethylureido)pyridine-4-carbothioamide (Intermediate 42, 0.146 g, 0.48 mmol) in acetonitrile (3 mL), 2-bromo-1-phenylethanone (0.105 g, 0.53 mmol) was added and the reaction mixture was heated to 80° for 16 h. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The resulting solids were filtered and washed with acetonitrile to yield 164 mg of the title compound as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674801B2
Source datasetuspto-grants-2010_03
ORD IDord-5f795704f2194ca29e815cfebf151739
Source noteuspto-grants-2010_03