Acetylglycine → N-({3-[(2S,4EZ)-1-([1,1'-biphenyl]-4-ylcarbonyl)-4-(methoxyimino)-pyrrolidinyl]-1,2,4-oxadiazol-5-yl}methyl)acetamide

HRID 1242565Notes

Reaction equation

HRID 1242565 reaction equation
[C:1]1([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:6]=[CH:5][C:4]([C:7]([N:9]2[CH2:13][C:12](=[N:14][O:15][CH3:16])[CH2:11][C@H:10]2[C:17](=[N:19][OH:20])[NH2:18])=[O:8])=[CH:3][CH:2]=1.[C:27]([NH:30][CH2:31][C:32](O)=O)(=[O:29])[CH3:28]>>[C:1]1([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:2]=[CH:3][C:4]([C:7]([N:9]2[CH2:13][C:12](=[N:14][O:15][CH3:16])[CH2:11][C@H:10]2[C:17]2[N:18]=[C:32]([CH2:31][NH:30][C:27](=[O:29])[CH3:28])[O:20][N:19]=2)=[O:8])=[CH:5][CH:6]=1

Participants

3

Procedure

Following the general method as outlined in Example 15, starting from (2S,4EZ)-1-([1,1′-biphenyl]-4-ylcarbonyl)-N′-hydroxy-4-(methoxyimino)-2-pyrrolidinecarboximidamide (Intermediate 8) and (acetylamino)acetic acid, the title compound was obtained in 72% purity by HPLC. MS(ESI+): m/z=434.2.

Sources & evidence

ORD record
ord-4ad9f3983fd046bd807c8f07b6adf302
Source dataset
uspto-grants-2006_10
Patent number
US07115639B2

Reaction notes

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