Benzenesulfonyl chloride → HCID 9952437, compound

HRID 1857943Notes

Reaction equation

HRID 1857943 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:13]=[C:12]([NH2:14])[N:11]=[C:10]([NH2:15])[N:9]=2)=[CH:4][CH:3]=1.[C:16]1([S:22](Cl)(=[O:24])=[O:23])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>>[NH2:14][C:12]1[N:11]=[C:10]([NH2:15])[N:9]=[C:8]([C:5]2[CH:4]=[CH:3][C:2]([NH:1][S:22]([C:16]3[CH:21]=[CH:20][C:19]4[C:18](=[CH:7][CH:2]=[CH:3][CH:4]=4)[CH:17]=3)(=[O:24])=[O:23])=[CH:7][CH:6]=2)[N:13]=1

Participants

3

Reactant 2

HCID 7369Benzenesulfonyl chlorideHCID 2748526-(4-aminophenyl)-1,3,5-triazine-2,4-diamine

Product 1

HCID 9952437HCID 9952437, compound

Procedure

6-(4-Aminophenyl)-1,3,5-triazine-2, 4diamine was processed as in Example 23 but substituting 2-naphthalenesulfonyl chloride for benzenesulfonyl chloride to provide the title compound.

Sources & evidence

ORD record
ord-87754ccdfcda4c67b20708c730e0eecf
Source dataset
uspto-grants-2000_11
Patent number
US06150362

Reaction notes

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