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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633022Generated: October 25, 2026

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

https://huagongshe.com/reaction/633022

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 numberUS09321761B2
Source datasetuspto-grants-2016_04
ORD IDord-6feebbc8861d4b5da3b074e8e21e8bf8
Source noteuspto-grants-2016_04