4-Nitrobenzoyl chloride → HCID 71075662, compound

HRID 2170612Notes

Reaction equation

HRID 2170612 reaction equation
[N+:1]([C:4]1[CH:12]=[CH:11][C:7]([C:8](Cl)=[O:9])=[CH:6][CH:5]=1)([O-:3])=[O:2].[C:13]1([CH:19]([NH:22][C:23]([C:25]2[CH:26]=[C:27]3[C:31](=[CH:32][CH:33]=2)[NH:30][CH:29]=[CH:28]3)=[O:24])[CH2:20][CH3:21])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[N+:1]([C:4]1[CH:12]=[CH:11][C:7]([C:8]([N:30]2[C:31]3[C:27](=[CH:26][C:25]([C:23]([NH:22][CH:19]([C:13]4[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=4)[CH2:20][CH3:21])=[O:24])=[CH:33][CH:32]=3)[CH:28]=[CH:29]2)=[O:9])=[CH:6][CH:5]=1)([O-:3])=[O:2]

Participants

3

Reactant 2

HCID 85024-Nitrobenzoyl chlorideHCID 63717133HCID 63717133, compound

Product 1

HCID 71075662HCID 71075662, compound

Procedure

The title compound was prepared following the same general protocol as described in Example 25, using 4-nitrobenzoylchloride and N-(1-phenylpropyl)-1H-indole-5-carboxamide. LC-MS 428 (M+H)

Sources & evidence

ORD record
ord-0ac5f1bcfbcf4bb7a144972f60795f78
Source dataset
uspto-grants-2015_06
Patent number
US09051265B2

Reaction notes

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