3-Phenyl-1,2-oxazole-5-carbaldehyde → HCID 58504029, compound

HRID 2407696Notes

Reaction equation

HRID 2407696 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]=1

Participants

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
US08809538B2

Reaction notes

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