Mandelic Acid → HCID 58729167, compound

HRID 1242577Notes

Reaction equation

HRID 1242577 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.[OH:27][CH:28]([C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)[C:29](O)=O>>[CH3:16][O:15][N:14]=[C:12]1[CH2:11][C@@H:10]([C:17]2[N:18]=[C:29]([CH:28]([OH:27])[C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)[O:20][N:19]=2)[N:9]([C:7]([C:4]2[CH:3]=[CH:2][C:1]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)=[CH:6][CH:5]=2)=[O:8])[CH2:13]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 (2RS)-hydroxy(phenyl)ethanoic acid, the title compound was obtained in 73% purity by HPLC. MS(ESI+): m/z=469.3.

Sources & evidence

ORD record
ord-efe44ca9ef074da3a277da0dc1e785e2
Source dataset
uspto-grants-2006_10
Patent number
US07115639B2

Reaction notes

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