4-Piperidin-1-yl-butylamine → HCID 18617705, compound

HRID 1264275Notes

Reaction equation

HRID 1264275 reaction equation
[N:1]1([CH2:7][CH2:8][CH2:9][CH2:10][NH2:11])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[C:12]([C:14]1[C:22]2[C:17](=[CH:18][CH:19]=[C:20]([CH2:23][CH2:24][NH:25][C:26](=[O:40])[C:27]3[CH:32]=[CH:31][C:30]([C:33]4[CH:38]=[CH:37][N:36]=[C:35](Cl)[N:34]=4)=[CH:29][CH:28]=3)[CH:21]=2)[NH:16][CH:15]=1)#[N:13]>>[C:12]([C:14]1[C:22]2[C:17](=[CH:18][CH:19]=[C:20]([CH2:23][CH2:24][NH:25][C:26](=[O:40])[C:27]3[CH:32]=[CH:31][C:30]([C:33]4[CH:38]=[CH:37][N:36]=[C:35]([NH:11][CH2:10][CH2:9][CH2:8][CH2:7][N:1]5[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]5)[N:34]=4)=[CH:29][CH:28]=3)[CH:21]=2)[NH:16][CH:15]=1)#[N:13]

Participants

3

Reactant 2

HCID 64841444-Piperidin-1-yl-butylamineHCID 18617562N-[2-(3-Cyano-1H-indol-5-yl)-ethyl]-4-[2-chloropyrimidin-4-yl]benzamide

Product 1

HCID 18617705HCID 18617705, compound

Procedure

Using 4-piperidin-1-ylbutylamine (reference example 93 g) and N-[2-(3-Cyano-1H-indol-5-yl)-ethyl]-4-[2-chloro-pyrimidin-4-yl]-benzamide (reference example 1az) as substrates. MS (ion spray) m/z 522 (M+H)+.

Sources & evidence

ORD record
ord-27741c6168264fb8a13974d72423e0fb
Source dataset
uspto-grants-2003_04
Patent number
US06541505B1

Reaction notes

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