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

HRID 1284821Notes

Reaction equation

HRID 1284821 reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([NH:9][S:10]([C:13]([F:16])([F:15])[F:14])(=[O:12])=[O:11])=[CH:4][C:3]=1[S:17](Cl)(=[O:19])=[O:18].[CH2:21]([NH2:24])[C:22]#[CH:23]>O1CCCC1>[CH2:21]([NH:24][S:17]([C:3]1[CH:4]=[C:5]([NH:9][S:10]([C:13]([F:16])([F:15])[F:14])(=[O:12])=[O:11])[C:6]([CH3:8])=[CH:7][C:2]=1[CH3:1])(=[O:19])=[O:18])[C:22]#[CH:23]

Participants

4

Procedure

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. M.P., 130.5°-132° C.

Workup

  1. customUpon completion of the reaction
  2. concentrationthe mixture was concentrated
  3. additionA 5% aqueous solution of hydrochloric acid was added to the residue, whereby an oily substance
  4. extractionThe oily substance was extracted with chloroform
  5. washwashed with a 5% aqueous solution of hydrochloric acid and water in order
  6. concentrationThe extract was concentrated
  7. customrecrystallized from toluene

Sources & evidence

ORD record
ord-5707fad6f3d24a43a92e8f1b456bd42b
Source dataset
uspto-grants-1986_01
Patent number
US04564386

Reaction notes

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