Trifluoromethylsulfonamide → HCID 86752963, compound

HRID 481425Notes

Reaction equation

HRID 481425 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.[F:29][C:30]([F:36])([F:35])[S:31]([NH2:34])(=[O:33])=[O:32]>>[F:29][C:30]([F:36])([F:35])[S:31]([NH2:34])(=[O:33])=[O:32].[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

3

Reactant 2

HCID 79001TrifluoromethylsulfonamideHCID 9952487HCID 9952487, compound

Product 1

HCID 86752963HCID 86752963, compound

Procedure

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

Sources & evidence

ORD record
ord-95995247906247c08e72976964cc24bc
Source dataset
uspto-grants-1998_08
Patent number
US05789415

Reaction notes

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