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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35498Generated: October 29, 2026

Propargylamine → N-propargyl-2,4-dimethyl-5-(trifluoromethanesulfonamido)benzenesulfonamide

https://huagongshe.com/reaction/35498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargylamineHCID 239041—
ReactantHCID 13300558HCID 13300558—
SolventTetrahydrofuranHCID 8028—
ProductN-propargyl-2,4-dimethyl-5-(trifluoromethanesulfonamido)benzenesulfonamideHCID 1330056666.5%

Reaction Steps

2,4-Dimethyl-5-(trifluoromethanesulfonamido)benzenesulfonyl chloride (1.5 g) was added to tetrahydrofuran (20 ml) containing propargylamine (0.5 g), and the resultant mixture was allowed to stand overnight at room temperature. Upon completion of the reaction, the mixture was concentrated. A 5% aqueous solution of hydrochloric acid was added to the residue, whereby an oily substance was deposited. The oily substance was extracted with chloroform and washed with a 5% aqueous solution of hydrochloric acid and water in order. The extract was concentrated and recrystallized from toluene to give 1.05 g of N-propargyl-2,4-dimethyl-5-(trifluoromethanesulfonamido)benzenesulfonamide (Compound No. 35). M.P., 130.5°-132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767446
Source datasetuspto-grants-1988_08
ORD IDord-1fa1d906d487453eaed9b357eea79a78
Source noteuspto-grants-1988_08