Acetamidine → HCID 178465678, compound

HRID 128412

Reaction equation

[C:1]([NH2:4])(=[NH:3])[CH3:2].[Cl:5][C:6]1[CH:17]=[CH:16][C:9]([CH:10]=[CH:11][S:12](Cl)(=[O:14])=[O:13])=[CH:8][CH:7]=1>>[Cl:5][C:6]1[CH:7]=[CH:8][C:9]([CH:10]=[CH:11][S:12]([NH:3][C:1](=[NH:4])[CH3:2])(=[O:14])=[O:13])=[CH:16][CH:17]=1

Participants

Reactant 2

HCID 67171Acetamidine

HCID 38443052-(4-chlorophenyl)ethenesulfonyl Chloride

Product 1

HCID 178465678HCID 178465678, compound

Procedure

Reaction of acetamidine with 4-chlorostyrylsulfonyl chloride according to the above procedure affords N-[(4-CHLOROSTYRYL)SULFONYL]ACETAMIDINE, m.p. 161°-163° C., crystallized from ethyl acetate.

Sources & evidence

ORD record: ord-f7372a3ca7d24e11a5bffa124d3417e5
Source dataset: uspto-grants-1981_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04259482

Linked notes

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