4-Nitrostyrylsulfonyl chloride → HCID 178513467, compound
Reaction equation
[CH:1]([C:9]1[CH:17]=[CH:16][C:12]([C:13]([NH2:15])=[NH:14])=[CH:11][CH:10]=1)=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[N+:18]([C:21]1[CH:32]=[CH:31][C:24]([CH:25]=[CH:26][S:27](Cl)(=[O:29])=[O:28])=[CH:23][CH:22]=1)([O-:20])=[O:19]>>[N+:18]([C:21]1[CH:22]=[CH:23][C:24]([CH:25]=[CH:26][S:27]([NH:14][C:13](=[NH:15])[C:12]2[CH:11]=[CH:10][C:9]([CH:1]=[CH:2][C:3]3[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=3)=[CH:17][CH:16]=2)(=[O:29])=[O:28])=[CH:31][CH:32]=1)([O-:20])=[O:19]Participants
3
Procedure
Reaction of 4-styrylbenzamidine with 4-nitrostyrylsulfonyl chloride according to the procedure of Example 29 (a) provides N-(4-NITROSTYRYLSULFONYL)-4-STYRYLBENZAMIDINE.
Sources & evidence
- ORD record
- ord-5a1c1786109548cfa9363e5c88a4a405
- Source dataset
- uspto-grants-1980_06
- Patent number
- US04206142
Reaction notes
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