3-Phenyl-1,2-oxazole-5-carbaldehyde → HCID 58504029, compound
Reaction equation
[C:1]1([C:7]2[C:11]3[C:12]([O:16][CH2:17][CH:18]4[CH2:23][CH2:22][NH:21][CH2:20][CH2:19]4)=[N:13][N:14]=[CH:15][C:10]=3[O:9][N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:24]1([C:30]2[CH:34]=[C:33]([CH:35]=O)[O:32][N:31]=2)[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>>[C:1]1([C:7]2[C:11]3[C:12]([O:16][CH2:17][CH:18]4[CH2:23][CH2:22][N:21]([CH2:35][C:33]5[O:32][N:31]=[C:30]([C:24]6[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=6)[CH:34]=5)[CH2:20][CH2:19]4)=[N:13][N:14]=[CH:15][C:10]=3[O:9][N:8]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
3
Procedure
According to the same procedure described in Example 35, using the compound obtained in Example 89 instead of the compound obtained in Example 11 and the compound obtained in Example 7 instead of 4-phenylthiophene-2-carbaldehyde, the title compound having the following physical data was obtained.
Sources & evidence
- ORD record
- ord-9cd72bb6b9d6418883fc7755b90804b8
- Source dataset
- uspto-grants-2014_08
- Patent number