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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272582Generated: October 27, 2026

Trifluoroacetic acid → N-(3-amino-2-methylpropyl)-4-cyanobenzenesulfonamide

https://huagongshe.com/reaction/2272582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86729742HCID 86729742—
ProductN-(3-amino-2-methylpropyl)-4-cyanobenzenesulfonamideHCID 8672974365.6%

Reaction Steps

A solution of the compound obtained in Step 1 (273 mg, 0.77 mmol) in TFA (1 mL, 12.98 mmol) was stirred at room temperature for min, and the mixture was concentrated under reduced pressure. To the residue were added ethyl acetate and 1N aqueous sodium hydroxide solution, and the organic layer was separated. The organic layer was washed with water and saturated brine, and dried, and the solvent was evaporated under reduced pressure to give N-(3-amino-2-methylpropyl)-4-cyanobenzenesulfonamide (128 mg, 0.505 mmol, 65.4%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120776B2
Source datasetuspto-grants-2015_09
ORD IDord-afeae13304ce47a6bbd456ef5cc0c1ba
Source noteuspto-grants-2015_09