4-Chloro-1,2-diaminobenzene → HCID 11656707, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([NH2:9])[C:5]([NH2:8])=[CH:6][CH:7]=1.[S:10]1[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=2[CH:12]=[C:11]1[S:19](Cl)(=[O:21])=[O:20]>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][S:19]([C:11]2[S:10][C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=3[CH:12]=2)(=[O:21])=[O:20])=[C:4]([NH:9][S:19]([C:11]2[S:10][C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=3[CH:12]=2)(=[O:20])=[O:21])[CH:3]=1Participants
3
Procedure
N,N′-(4-chloro-1,2-phenylene)bis(1-benzothiophene-2-sulfonamide) (310 mg) was prepared as in Example 31 using 4-chlorobenzene-1,2-diamine and benzothiophene-2-sulfonyl chloride as requisite starting materials.
Sources & evidence
- ORD record
- ord-203249a7db0e46da906554fd852d7d7c
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07582673B2
Reaction notes
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