4-[4-(tert-Butyl)-1,3-thiazol-2-yl]benzaldehyde → HCID 22048888, compound
Reaction equation
[C:1]([C:5]1[N:6]=[C:7]([C:10]2[CH:17]=[CH:16][C:13]([CH:14]=O)=[CH:12][CH:11]=2)[S:8][CH:9]=1)([CH3:4])([CH3:3])[CH3:2].[CH3:18][CH:19]([CH3:35])[C:20]([NH:22][C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([CH:29]2[CH2:34][CH2:33][NH:32][CH2:31][CH2:30]2)[CH:24]=1)=[O:21]>>[C:1]([C:5]1[N:6]=[C:7]([C:10]2[CH:17]=[CH:16][C:13]([CH2:14][N:32]3[CH2:33][CH2:34][CH:29]([C:25]4[CH:24]=[C:23]([NH:22][C:20](=[O:21])[CH:19]([CH3:18])[CH3:35])[CH:28]=[CH:27][CH:26]=4)[CH2:30][CH2:31]3)=[CH:12][CH:11]=2)[S:8][CH:9]=1)([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
Prepared by Procedure F and Scheme R using 4-(4-tert-butyl-1,3-thiazol-2-yl)benzaldehyde and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide.
Workup
- customPrepared by Procedure F and Scheme R
Sources & evidence
- ORD record
- ord-505620253be84dff81c7cf295a35f5db
- Source dataset
- uspto-grants-2006_06
- Patent number
- US07067534B1
Reaction notes
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