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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887684Generated: October 25, 2026

Trifluoroacetic acid → N-(3-(aminomethyl)pyridin-2-yl)-N-methylmethanesulfonamide

https://huagongshe.com/reaction/1887684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-butyl (2-(N-methylmethylsulfonamido)pyridin-3-yl)methylcarbamateHCID 58155014—
SolventDichloromethaneHCID 6344—
ProductN-(3-(aminomethyl)pyridin-2-yl)-N-methylmethanesulfonamideHCID 4548040388.5%

Reaction Steps

To a 25 mL round bottom flask charged with tert-butyl (2-(N-methylmethylsulfonamido)pyridin-3-yl)methylcarbamate (118 mg, 0.26 mmol) was added a 40% solution of TFA in CH2Cl2 (4 mL). The resulting mixture was stirred for 20 min, then the volatiles were evaporated. Toluene (4 mL) was added to the crude followed by evaporation. This procedure was repeated once. A solution of the crude residue in CH2Cl2 (4 mL) was treated with Amberlyst A-21 (1.8 g) and stirred for 30 min. The Amberlyst A-21 resin was filtered off and washed with CH2Cl2 (20 mL). The volatiles were evaporated to yield N-(3-(aminomethyl)pyridin-2-yl)-N-methylmethanesulfonamide (50 mg, 0.23 mmol, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501763B2
Source datasetuspto-grants-2013_08
ORD IDord-951da8c396884dfba254800298464a49
Source noteuspto-grants-2013_08