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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117950Generated: October 30, 2026

Dichloromethane → HCID 21915000, compound

https://huagongshe.com/reaction/2117950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 21914707HCID 21914707—
SolventWaterHCID 962—
SolventChloroform methanolHCID 21584188—
ProductHCID 21915000HCID 21915000—

Reaction Steps

N-(4-{4-[(2-Hydroxyethyl)sulfonyl]phenyl}-1,3-thiazol-2-yl)acetamide (200 mg), Et3N (0.102 ml) and CH2Cl2 (4 ml) were combined under N2 atmosphere, and then MsCl (0.05 ml) was added to the suspension at 0° C. The reaction mixture was stirred at r.t. for 2 hours. MeOH/CHCl3 and water were added to the mixture, and the mixture was extracted. The organic layer was washed with brine, dried over anhydrous MgSO4, and concentrated in vacuo. The residual solid (221.6 mg) was suspended in CH3CN (10 ml), and then 28% ammonia solution (0.5 ml) was added to the suspension at 0° C. The reaction mixture was stirred at r.t. for 15 hours, and concentrated in vacuo. The residue was purified by flash column chromatography over silica gel with [MeOH/CHCl3 (1:30), then NH4OH/MeOH/CHCl3 (1:10:60)] as an eluent, and triturated with EtOH/ethyl ether to give N-(4-{4-[(2-aminoethyl)sulfonyl]phenyl}-1,3-thiazol-2-yl)acetamide (60.4 mg) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442715B2
Source datasetuspto-grants-2008_10
ORD IDord-8c858cca78a74965953b804dcaa2883f
Source noteuspto-grants-2008_10