HCID 59152645, compound → 4-[6-(2-Isopropoxy-ethoxy)-benzofuran-3-ylmethoxy]-1H-indole-2-carboxylic acid {4-hydroxy-4-[2-((3S,4S)-4-hydroxy-3-methyl-piperidin-1-yl)-ethyl]-cyclohexyl}-amide

HRID 1804809Notes

Reaction equation

HRID 1804809 reaction equation
[CH:1]([O:4][CH2:5][CH2:6][O:7][C:8]1[CH:30]=[CH:29][C:11]2[C:12]([CH2:15][O:16][C:17]3[CH:25]=[CH:24][CH:23]=[C:22]4[C:18]=3[CH:19]=[C:20]([C:26]([OH:28])=O)[NH:21]4)=[CH:13][O:14][C:10]=2[CH:9]=1)([CH3:3])[CH3:2].[NH2:31][CH:32]1[CH2:37][CH2:36][C:35]([CH2:39][CH2:40][N:41]2[CH2:46][CH2:45][C@H:44]([OH:47])[C@@H:43]([CH3:48])[CH2:42]2)([OH:38])[CH2:34][CH2:33]1>>[OH:38][C:35]1([CH2:39][CH2:40][N:41]2[CH2:46][CH2:45][C@H:44]([OH:47])[C@@H:43]([CH3:48])[CH2:42]2)[CH2:36][CH2:37][CH:32]([NH:31][C:26]([C:20]2[NH:21][C:22]3[C:18]([CH:19]=2)=[C:17]([O:16][CH2:15][C:12]2[C:11]4[CH:29]=[CH:30][C:8]([O:7][CH2:6][CH2:5][O:4][CH:1]([CH3:2])[CH3:3])=[CH:9][C:10]=4[O:14][CH:13]=2)[CH:25]=[CH:24][CH:23]=3)=[O:28])[CH2:33][CH2:34]1

Participants

3

Procedure

This compound is synthesized analogously to example 1 from 4-[6-(2-Isopropoxy-ethoxy)-benzofuran-3-ylmethoxy]-1H-indole-2-carboxylic acid 30e and amine 14.

Sources & evidence

ORD record
ord-85e96bebd7034961aaeb6e3253e9d279
Source dataset
uspto-grants-2013_01
Patent number
US08354431B2

Reaction notes

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