p-Toluenesulfonic acid → 1-Dimethylaminosulfonyl-2-amino-6-(alpha-isopropylidenbenzyl)benzimidazole

HRID 435486Notes

Reaction equation

HRID 435486 reaction equation
[CH3:1][N:2]([CH3:27])[S:3]([N:6]1[C:10]2[CH:11]=[C:12]([C:15]([CH:23]([CH3:25])[CH3:24])(O)[C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[CH:13]=[CH:14][C:9]=2[N:8]=[C:7]1[NH2:26])(=[O:5])=[O:4].C1(C)C=CC(S(O)(=O)=O)=CC=1>C(Cl)(Cl)Cl>[CH3:27][N:2]([CH3:1])[S:3]([N:6]1[C:10]2[CH:11]=[C:12]([C:15](=[C:23]([CH3:24])[CH3:25])[C:16]3[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=3)[CH:13]=[CH:14][C:9]=2[N:8]=[C:7]1[NH2:26])(=[O:4])=[O:5]

Participants

4

Procedure

When the procedure of Example 72 was repeated using 1.2 g. (3.2 mmoles) of 1-dimethylaminosulfonyl-2-amino-6-(α-isopropyl-α-hydroxybenzyl)benzimidazole, 750 mg. of p-toluenesulfonic acid, and 100 ml. of chloroform, there was obtained 1-dimethylaminosulfonyl-2-amino-6-(α-isopropylidenebenzyl)benzimidazole.

Sources & evidence

ORD record
ord-c7800da0d7674eccac84bcb45ee0373b
Source dataset
uspto-grants-1983_08
Patent number
US04401817

Reaction notes

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