Cyclohexylamine → HCID 54450918, compound

HRID 66917Notes

Reaction equation

HRID 66917 reaction equation
Cl.[CH3:2][C:3]([O:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[N:14]([CH2:18][CH2:19][CH3:20])[C:13]([CH3:21])=[C:12]2[C:22]1[CH:27]=[CH:26][N:25]=[CH:24][CH:23]=1)([CH3:7])[C:4](O)=[O:5].[CH:28]1([NH2:34])[CH2:33][CH2:32][CH2:31][CH2:30][CH2:29]1>>[CH:28]1([NH:34][C:4](=[O:5])[C:3]([CH3:7])([O:8][C:9]2[CH:10]=[C:11]3[C:15](=[CH:16][CH:17]=2)[N:14]([CH2:18][CH2:19][CH3:20])[C:13]([CH3:21])=[C:12]3[C:22]2[CH:23]=[CH:24][N:25]=[CH:26][CH:27]=2)[CH3:2])[CH2:33][CH2:32][CH2:31][CH2:30][CH2:29]1

Participants

3

Reactant 2

HCID 7965CyclohexylamineHCID 3059433Propanoic acid, 2-methyl-2-((2-methyl-1-propyl-3-(4-pyridinyl)-1H-indol-5-yl)oxy)-, hydrochloride

Product 1

HCID 54450918HCID 54450918, compound

Procedure

In accordance with a procedure analogous to that of Example 128, the above compound was prepared from 2-methyl-2-[2-methyl-1-propyl-3-(4-pyridyl)-1H-indole-5-yloxy]propanoic acid hydrochloride and cyclohexylamine.

Sources & evidence

ORD record
ord-3849eebc17dd4605a074c6321edd1ddb
Source dataset
uspto-grants-1982_08
Patent number
US04343811

Reaction notes

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