Methanesulfonyl chloride → HCID 18419552, compound

HRID 1594777Notes

Reaction equation

HRID 1594777 reaction equation
[C:1]([C:5]1[CH:6]=[C:7]([CH:24]=[C:25]([C:28]([CH3:31])([CH3:30])[CH3:29])[C:26]=1[OH:27])[CH2:8][N:9]([C:18]1[CH:19]=[N:20][CH:21]=[CH:22][CH:23]=1)[S:10]([C:13]1SC=CC=1)(=[O:12])=[O:11])([CH3:4])([CH3:3])[CH3:2].S1C=CC=C1S(Cl)(=O)=O.CS(Cl)(=O)=O>>[C:1]([C:5]1[CH:6]=[C:7]([CH:24]=[C:25]([C:28]([CH3:31])([CH3:30])[CH3:29])[C:26]=1[OH:27])[CH2:8][N:9]([C:18]1[CH:19]=[N:20][CH:21]=[CH:22][CH:23]=1)[S:10]([CH3:13])(=[O:12])=[O:11])([CH3:4])([CH3:3])[CH3:2]

Participants

4

Procedure

This compound was prepared in the same manner as for the title compound of Example 7, except the 2-thiophene sulfonyl chloride was replaced with methane sulfonyl chloride.

Sources & evidence

ORD record
ord-9dc101a33a2748e18621827339d366f4
Source dataset
uspto-grants-2001_09
Patent number
US06284795B1

Reaction notes

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