5-(2-pyrrolidin-1-yl-ethoxy)-1H-indole-2-carbaldehyde → HCID 69586825, compound

HRID 49093Notes

Reaction equation

HRID 49093 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([NH:7][S:8]([C:11]2[CH:12]=[C:13]3[C:17](=[CH:18][CH:19]=2)[NH:16][C:15](=[O:20])[CH2:14]3)(=[O:10])=[O:9])[CH:2]=1.[N:21]1([CH2:26][CH2:27][O:28][C:29]2[CH:30]=[C:31]3[C:35](=[CH:36][CH:37]=2)[NH:34][C:33]([CH:38]=O)=[CH:32]3)[CH2:25][CH2:24][CH2:23][CH2:22]1>>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([NH:7][S:8]([C:11]2[CH:12]=[C:13]3[C:17](=[CH:18][CH:19]=2)[NH:16][C:15](=[O:20])[C:14]3=[CH:38][C:33]2[NH:34][C:35]3[C:31]([CH:32]=2)=[CH:30][C:29]([O:28][CH2:27][CH2:26][N:21]2[CH2:25][CH2:24][CH2:23][CH2:22]2)=[CH:37][CH:36]=3)(=[O:10])=[O:9])[CH:2]=1

Participants

3

Procedure

2-Oxo-2,3-dihydro-1H-indole-5-sulfonic acid pyridin-3-ylamide was condensed with 5-(2-pyrrolidin-1-yl-ethoxy)-1H-indole-2-carbaldehyde to give the title compound.

Sources & evidence

ORD record
ord-5ec641b27d29475eb6ddcfcfd4f302f5
Source dataset
uspto-grants-2004_03
Patent number
US06706709B2

Reaction notes

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