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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750052Generated: November 1, 2026

Chloroform → (3-Bromo-5-trifluoromethylsulfanylpyridine-2-yl)-methylamine

https://huagongshe.com/reaction/1750052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantN-bromobutanimideHCID 67184—
ReactantN-Methyl-5-((trifluoromethyl)thio)pyridin-2-amineHCID 67982149—
SolventWaterHCID 962—
Product(3-Bromo-5-trifluoromethylsulfanylpyridine-2-yl)-methylamineHCID 6798126793.5%

Reaction Steps

1.43 g of N-bromosuccinimide was added to a mixture of 1.52 g of methyl-(5-trifluoromethylsulfanylpyridin-2-yl)-amine and 24 ml of chloroform, and the mixture was stirred at room temperature for 1 hour. Water was added to the reaction mixture, and the mixture was extracted with chloroform. The combined organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 1.96 g of (3-bromo-5-trifluoromethylsulfanylpyridin-2-yl)-methylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156838B2
Source datasetuspto-grants-2015_10
ORD IDord-1c018e04ea034546a5b707024be217be
Source noteuspto-grants-2015_10