3,5-Dimethylpiperidine → HCID 22638565, compound

HRID 2416228Notes

Reaction equation

HRID 2416228 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.[CH3:25][CH:26]1[CH2:31][CH:30]([CH3:32])[CH2:29][NH:28][CH2:27]1>>[CH3:25][CH:26]1[CH2:31][CH:30]([CH3:32])[CH2:29][N:28]([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)[CH2:27]1

Participants

3

Reactant 2

HCID 1182593,5-DimethylpiperidineHCID 22638533HCID 22638533, compound

Product 1

HCID 22638565HCID 22638565, 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 3,5-dimethylpiperidine to give a yellow solid. MS m/z: 431.1 (M+1).

Workup

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

Sources & evidence

ORD record
ord-2ecd1915964d4bbfa259a21c123c7122
Source dataset
uspto-grants-2004_11
Patent number
US06822097B1

Reaction notes

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