Acetaldehyde → HCID 135520170, compound
Reaction equation
[C:1]([C:4]1[CH:5]=[C:6]([C:14]2[NH:15][C:16](=[O:31])[C:17]3[C:18](=[C:20]([CH2:29][CH3:30])[N:21]([CH:23]4[CH2:28][CH2:27][NH:26][CH2:25][CH2:24]4)[N:22]=3)[N:19]=2)[C:7]([O:10][CH2:11][CH2:12][CH3:13])=[N:8][CH:9]=1)(=[O:3])[CH3:2].[CH:32](=O)[CH3:33]>>[C:1]([C:4]1[CH:5]=[C:6]([C:14]2[NH:15][C:16](=[O:31])[C:17]3[C:18](=[C:20]([CH2:29][CH3:30])[N:21]([CH:23]4[CH2:24][CH2:25][N:26]([CH2:32][CH3:33])[CH2:27][CH2:28]4)[N:22]=3)[N:19]=2)[C:7]([O:10][CH2:11][CH2:12][CH3:13])=[N:8][CH:9]=1)(=[O:3])[CH3:2]Participants
3
Procedure
The title compound was prepared by the method of example 51 using the title compound of example 118 and acetaldehyde.
Sources & evidence
- ORD record
- ord-c4cef8b1c01445e2bcef19ba011618cd
- Source dataset
- uspto-grants-2004_06
- Patent number
- US06756373B1
Reaction notes
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