1-(2-(Azepan-1-yl)ethyl)piperidin-4-amine trihydrochloride → HCID 11154545, compound

HRID 1929024Notes

Reaction equation

HRID 1929024 reaction equation
[CH:1]([O:4][C:5]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:6]=1[CH:7]=[C:8]([C:14]([OH:16])=O)[NH:9]2)([CH3:3])[CH3:2].Cl.Cl.Cl.[N:20]1([CH2:27][CH2:28][N:29]2[CH2:34][CH2:33][CH:32]([NH2:35])[CH2:31][CH2:30]2)[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1>>[N:20]1([CH2:27][CH2:28][N:29]2[CH2:30][CH2:31][CH:32]([NH:35][C:14]([C:8]3[NH:9][C:10]4[C:6]([CH:7]=3)=[C:5]([O:4][CH:1]([CH3:2])[CH3:3])[CH:13]=[CH:12][CH:11]=4)=[O:16])[CH2:33][CH2:34]2)[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1

Participants

3

Reactant 2

HCID 668413931-(2-(Azepan-1-yl)ethyl)piperidin-4-amine trihydrochlorideHCID 66841602HCID 66841602, compound

Product 1

HCID 11154545HCID 11154545, compound

Procedure

This compound is synthesized analogously to Example 1 from 4-Isopropoxy-1H-indole-2-carboxylic acid 74 (preparation see below) and amine 5.

Sources & evidence

ORD record
ord-26735f3bf6e9410da9ff5524f193ab28
Source dataset
uspto-grants-2012_05
Patent number
US08183366B2

Reaction notes

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