4-Isobutoxy-1H-indole-2-carboxylic acid [1-(2-azepan-1-yl-ethyl)-piperidin-4-yl]-amide → 4-Isobutoxy-1H-indole-2-carboxylic acid [1-(2-piperidin-1-yl-ethyl)-piperidin-4-yl]-amide

HRID 2267740Notes

Reaction equation

HRID 2267740 reaction equation
[N:1]1([CH2:8][CH2:9][N:10]2[CH2:15][CH2:14][CH:13]([NH:16][C:17]([C:19]3[NH:20][C:21]4[C:26]([CH:27]=3)=[C:25]([O:28][CH2:29][CH:30]([CH3:32])[CH3:31])[CH:24]=[CH:23][CH:22]=4)=[O:18])[CH2:12][CH2:11]2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]C1.Cl.Cl.Cl.N1(CCN2CCC(N)CC2)CCCCC1>>[N:1]1([CH2:8][CH2:9][N:10]2[CH2:15][CH2:14][CH:13]([NH:16][C:17]([C:19]3[NH:20][C:21]4[C:26]([CH:27]=3)=[C:25]([O:28][CH2:29][CH:30]([CH3:32])[CH3:31])[CH:24]=[CH:23][CH:22]=4)=[O:18])[CH2:12][CH2:11]2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1

Participants

3

Reactant 2

HCID 114420474-Isobutoxy-1H-indole-2-carboxylic acid [1-(2-azepan-1-yl-ethyl)-piperidin-4-yl]-amideHCID 668413621-(2-(Piperidin-1-yl)ethyl)piperidin-4-amine trihydrochloride

Product 1

HCID 114076754-Isobutoxy-1H-indole-2-carboxylic acid [1-(2-piperidin-1-yl-ethyl)-piperidin-4-yl]-amide

Procedure

This compound is synthesized analogously to Example 1 from 4-Isobutoxy-1H-indole-2-carboxylic acid 80 (preparation see Example 8) and amine 1.

Sources & evidence

ORD record
ord-e7ba53b6acf44cb2b968a81f90953d9c
Source dataset
uspto-grants-2010_12
Patent number
US07858781B2

Reaction notes

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