N-Acetylsulfanilyl chloride → HCID 14152359, compound

HRID 1608161Notes

Reaction equation

HRID 1608161 reaction equation
[NH2:1][CH2:2][CH2:3][C:4]1[N:5]([CH3:9])[CH:6]=[CH:7][CH:8]=1.[C:10]([NH:13][C:14]1[CH:19]=[CH:18][C:17]([S:20](Cl)(=[O:22])=[O:21])=[CH:16][CH:15]=1)(=[O:12])[CH3:11]>>[C:10]([NH:13][C:14]1[CH:15]=[CH:16][C:17]([S:20]([NH:1][CH2:2][CH2:3][C:4]2[N:5]([CH3:9])[CH:6]=[CH:7][CH:8]=2)(=[O:22])=[O:21])=[CH:18][CH:19]=1)(=[O:12])[CH3:11]

Participants

3

Reactant 2

HCID 8481N-Acetylsulfanilyl chlorideHCID 5650581-methyl-1H-pyrrole-2-ethylamine

Product 1

HCID 14152359HCID 14152359, compound

Procedure

Prepared from 2-(2-aminoethyl)-1-methylpyrrol and p-acetamidobenzenesulphonylchloride analogously to Example A.

Sources & evidence

ORD record
ord-67447a7d3aa941db92e25640050aac70
Source dataset
uspto-grants-1989_09
Patent number
US04870076

Reaction notes

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