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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436410Generated: November 3, 2026

Dichloromethane → N-[4-(4-bromophenyl)-1,3-thiazol-2-yl]-2-hydroxyacetamide

https://huagongshe.com/reaction/1436410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactant2-{[4-(4-Bromophenyl)-1,3-thiazol-2-yl]amino}-2-oxoethyl acetateHCID 86618604—
SolventMethanolHCID 887—
ProductN-[4-(4-bromophenyl)-1,3-thiazol-2-yl]-2-hydroxyacetamideHCID 79023069%

Reaction Steps

2-{[4-(4-Bromophenyl)-1,3-thiazol-2-yl]amino}-2-oxoethyl acetate (1.1 g, 3.1 mmol), prepared in the previous step, was suspended in 20 mL of methanol and K2CO3 (0.43 g, 3.1 mmol) was added. The mixture was stirred for 2 h, then diluted using methylene chloride. The mixture was washed with water, brine, dried over anhydrous MgSO4, filtered and concentrated under reduced pressure. Flash chromatography (2% methanol/chloroform) provided N-[4-(4-bromophenyl)-1,3-thiazol-2-yl]-2-hydroxyacetamide (670 mg, 68%) as a white solid. mp 222-224° C. HRMS: calcd for C11H9BrN2O2S+H+, 312.96408; found (ESI, [M+H]+), 312.9651. Analytical HPLC: retention time 9.0 min, 210-370 nm the Xterra® RP18 column, 3.5μ, 150×4.6 mm 40° C. 85/15-5/95 (Ammon. Form. Buff. pH=3.5/ACN+MeOH) for 10 min, hold 4 min, 1.2 mL/min 5 μL injection.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618990B2
Source datasetuspto-grants-2009_11
ORD IDord-eecb1eeb59564dcc8725ccceb39d3303
Source noteuspto-grants-2009_11