Cyclopentylamine → HCID 22638630, compound

HRID 2416231Notes

Reaction equation

HRID 2416231 reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([C:7]2[S:8][CH:9]=[C:10]([C:12]3[C:13](=[O:24])[NH:14][C:15]4[C:20]([CH:21]=3)=[CH:19][CH:18]=[C:17]([CH:22]=O)[CH:16]=4)[N:11]=2)=[CH:3][CH:2]=1.[CH:25]1([NH2:30])[CH2:29][CH2:28][CH2:27][CH2:26]1>>[CH:25]1([NH:30][CH2:22][C:17]2[CH:16]=[C:15]3[C:20]([CH:21]=[C:12]([C:10]4[N:11]=[C:7]([C:4]5[CH:5]=[CH:6][N:1]=[CH:2][CH:3]=5)[S:8][CH:9]=4)[C:13](=[O:24])[NH:14]3)=[CH:19][CH:18]=2)[CH2:29][CH2:28][CH2:27][CH2:26]1

Participants

3

Reactant 2

HCID 2906CyclopentylamineHCID 22638533HCID 22638533, compound

Product 1

HCID 22638630HCID 22638630, compound

Procedure

This compound was prepared according to the method described in example 8768 employing 3-(2-pyridin-4-yl-thiazol-4-yl)-1H-quinolin-2-one-7-carbaldehyde and cyclopentylamine to give a yellow solid. MS m/z: 403.2 (M+1).

Workup

  1. customThis compound was prepared
  2. customto give a yellow solid

Sources & evidence

ORD record
ord-cdf094dc1be54d56845dc9aea847bd54
Source dataset
uspto-grants-2004_11
Patent number
US06822097B1

Reaction notes

Loading…