3-Nitrobenzamidine → HCID 178513468, compound

HRID 1706084Notes

Reaction equation

[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][CH:12]=1)[C:7]([NH2:9])=[NH:8])([O-:3])=[O:2].[N+:13]([C:16]1[CH:27]=[CH:26][C:19]([CH:20]=[CH:21][S:22](Cl)(=[O:24])=[O:23])=[CH:18][CH:17]=1)([O-:15])=[O:14]>>[N+:13]([C:16]1[CH:17]=[CH:18][C:19]([CH:20]=[CH:21][S:22]([NH:8][C:7](=[NH:9])[C:6]2[CH:10]=[CH:11][CH:12]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=2)(=[O:24])=[O:23])=[CH:26][CH:27]=1)([O-:15])=[O:14]

Participants

Reactant 2

HCID 1651223-Nitrobenzamidine

HCID 3480064-Nitrostyrylsulfonyl chloride

Product 1

HCID 178513468HCID 178513468, compound

Procedure

Reaction of 3-nitrobenzamidine with 4-nitrostyrylsulfonyl chloride according to the above procedure provides N-(4-NITROSTYRYLSULFONYL)-3-NITROBENZAMIDINE, m.p. 230°-232° C.

Sources & evidence

ORD record: ord-a42c32f59f7842e4bea08659ebbee97b
Source dataset: uspto-grants-1980_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04206142

Reaction notes

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