O-Phenylenediamine → HCID 54436784, compound

HRID 612671Notes

Reaction equation

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

Participants

Reactant 2

HCID 7243O-Phenylenediamine

HCID 8481N-Acetylsulfanilyl chloride

Product 1

HCID 54436784HCID 54436784, compound

Procedure

The sulfonamide was synthesized from 4-acetamidophenyl sulfonyl chloride (0.01 mol) and o-phenylene diamine (0.01 mmol) by general Method C. It was purified by recrystallization from EtOH (1.27 g, 40%) EI-MS m/z 304 (M-H)-.

Workup

customIt was purified by recrystallization from EtOH (1.27 g, 40%) EI-MS m/z 304 (M-H)-

Sources & evidence

ORD record: ord-3e586d5f1da148ebac9d0abc7b623efd
Source dataset: uspto-grants-1999_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06005008

Reaction notes

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