Methanesulfonamide → HCID 86752962, compound

HRID 481424Notes

Reaction equation

[CH:1]1([C:4]2[N:14]([CH2:15][C:16]3[S:20][C:19]([C:21]4([C:26]([OH:28])=[O:27])[CH2:25][CH:24]=[CH:23][CH2:22]4)=[CH:18][CH:17]=3)[C:7]3=[N:8][C:9]([CH3:13])=[CH:10][C:11]([CH3:12])=[C:6]3[N:5]=2)[CH2:3][CH2:2]1.[CH3:29][S:30]([NH2:33])(=[O:32])=[O:31]>>[CH3:29][S:30]([NH2:33])(=[O:32])=[O:31].[CH:1]1([C:4]2[N:14]([CH2:15][C:16]3[S:20][C:19]([C:21]4([C:26]([OH:28])=[O:27])[CH2:25][CH:24]=[C:23]=[CH:22]4)=[CH:18][CH:17]=3)[C:7]3=[N:8][C:9]([CH3:13])=[CH:10][C:11]([CH3:12])=[C:6]3[N:5]=2)[CH2:2][CH2:3]1

Participants

Reactant 2

HCID 72879Methanesulfonamide

HCID 9952487HCID 9952487, compound

Product 1

HCID 86752962HCID 86752962, compound

Procedure

The title compound was prepared from the product of Example 3, above, by the method of Example 25, except that methanesulfonamide was used in place of benzenesulfonamide.

Sources & evidence

ORD record: ord-2a1ae23b948d4859ab8d07d6a889adda
Source dataset: uspto-grants-1998_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05789415

Reaction notes

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