1-Naphthalenesulfonyl chloride → HCID 71075876, compound

HRID 2170615Notes

Reaction equation

HRID 2170615 reaction equation
[C:1]1([S:11](Cl)(=[O:13])=[O:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[C:15]1([CH:21]([NH:24][C:25]([C:27]2[CH:28]=[C:29]3[C:33](=[CH:34][CH:35]=2)[NH:32][CH:31]=[CH:30]3)=[O:26])[CH2:22][CH3:23])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[C:1]1([S:11]([N:32]2[C:33]3[C:29](=[CH:28][C:27]([C:25]([NH:24][CH:21]([C:15]4[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=4)[CH2:22][CH3:23])=[O:26])=[CH:35][CH:34]=3)[CH:30]=[CH:31]2)(=[O:13])=[O:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1

Participants

3

Reactant 2

HCID 665601-Naphthalenesulfonyl chlorideHCID 63717133HCID 63717133, compound

Product 1

HCID 71075876HCID 71075876, compound

Procedure

The title compound was prepared following the same general protocol as described in Example 28, using 1-naphthylsulfonyl chloride and N-(1-phenylpropyl)-1H-indole-5-carboxamide. LC-MS 469 (M+H).

Sources & evidence

ORD record
ord-d9233a6372f841058acc54077d1302ab
Source dataset
uspto-grants-2015_06
Patent number
US09051265B2

Reaction notes

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