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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038447Generated: October 31, 2026

Chloroacetaldehyde → N-(3-(thiazol-2-ylamino)phenyl)methanesulfonamide

https://huagongshe.com/reaction/1038447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
ReactantN-(3-thioureidophenyl)methanesulfonamideHCID 86674185—
SolventEthanolHCID 702—
ProductN-(3-(thiazol-2-ylamino)phenyl)methanesulfonamideHCID 8667418493.4%

Reaction Steps

N-(3-thioureidophenyl)methanesulfonamide 54 (1.14 g, 4.65 mmol) and 50% aq. chloroacetaldehyde solution (3.65 mL, 23.25 mmol) were taken into ethanol and refluxed for 2 hours. Reaction mixture was concentrated and aq. Saturated NaHCO3 was added. Resulting light brown solid was filtered and washed with water, dried under high vacuum to obtain N-(3-(thiazol-2-ylamino)phenyl)methanesulfonamide 55 (1.17 g, 93% yield). Resulting product was further used without further purification. MS (ES) m/z 270 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551992B2
Source datasetuspto-grants-2013_10
ORD IDord-e2089bbe94b646fd901ae8a889e4f880
Source noteuspto-grants-2013_10