4-Nitrobenzenesulfonyl chloride → HCID 71075612, compound

HRID 2170616Notes

Reaction equation

HRID 2170616 reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([S:10](Cl)(=[O:12])=[O:11])=[CH:6][CH:5]=1)([O-:3])=[O:2].[C:14]1([CH:20]([NH:23][C:24]([C:26]2[CH:27]=[C:28]3[C:32](=[CH:33][CH:34]=2)[NH:31][CH:30]=[CH:29]3)=[O:25])[CH2:21][CH3:22])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>>[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([S:10]([N:31]2[C:32]3[C:28](=[CH:27][C:26]([C:24]([NH:23][CH:20]([C:14]4[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=4)[CH2:21][CH3:22])=[O:25])=[CH:34][CH:33]=3)[CH:29]=[CH:30]2)(=[O:12])=[O:11])=[CH:6][CH:5]=1)([O-:3])=[O:2]

Participants

3

Reactant 2

HCID 74044-Nitrobenzenesulfonyl chlorideHCID 63717133HCID 63717133, compound

Product 1

HCID 71075612HCID 71075612, compound

Procedure

The title compound was prepared following the same general protocol as described in Example 28, using 4-nitrophenylsulfonyl chloride and N-(1-phenylpropyl)-1H-indole-5-carboxamide. LC-MS 464 (M+H).

Sources & evidence

ORD record
ord-3fdbf55c819648cc9a052a3c4d3356c9
Source dataset
uspto-grants-2015_06
Patent number
US09051265B2

Reaction notes

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