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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364648Generated: October 25, 2026

Chlorosuccinimide → N-benzyl-5-chloro-4-(pyridin-2-yl)thiazol-2-amine

https://huagongshe.com/reaction/1364648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantN-benzyl-4-(pyridin-2-yl)thiazol-2-amineHCID 2902584—
SolventDimethylformamideHCID 6228—
ProductN-benzyl-5-chloro-4-(pyridin-2-yl)thiazol-2-amineHCID 58614641—

Reaction Steps

A solution of N-benzyl-4-(pyridin-2-yl)thiazol-2-amine (60 mg, 0.23 mmol) in DMF (2 mL) was cooled to 0° C. and treated with N-chlorosuccinimide (33 mg, 0.25 mmol), and the reaction mixture was allowed to warm to room temperature. The solvent was evaporated, and the product was purified on reverse phase HPLC to produce N-benzyl-5-chloro-4-(pyridin-2-yl)thiazol-2-amine. MS (Q1) 302.2 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888364B2
Source datasetuspto-grants-2011_02
ORD IDord-8233f7d92a354f708951ac2c74f968d1
Source noteuspto-grants-2011_02