Serinol → HCID 131725653, compound

HRID 1745325Notes

Reaction equation

HRID 1745325 reaction equation
C(O[C:6]([N:8]1[CH2:12][C:11](=[N:13][O:14][CH3:15])[CH2:10][C@H:9]1[C:16]([OH:18])=O)=[O:7])(C)(C)C.[CH3:19][C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([CH3:26])[C:21]=1[C:27]1[CH:32]=[CH:31][C:30](C(O)=O)=[CH:29][CH:28]=1.[NH2:36][CH:37]([CH2:40][OH:41])[CH2:38][OH:39]>>[CH3:26][C:22]1[CH:23]=[CH:24][CH:25]=[C:20]([CH3:19])[C:21]=1[C:27]1[CH:28]=[CH:29][C:30]([C:6]([N:8]2[CH2:12][C:11](=[N:13][O:14][CH3:15])[CH2:10][C@H:9]2[C:16]([NH:36][CH:37]([CH2:40][OH:41])[CH2:38][OH:39])=[O:18])=[O:7])=[CH:31][CH:32]=1

Participants

4

Procedure

Following the general method as outlined in Example 22, starting from (2S,4EZ)-1-(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidinecarboxylic acid, 2′,6′-dimethyl[1,1′-biphenyl]-4-carboxylic acid, and 2-amino-1,3-propanediol, the title compound was obtained in 70% purity by HPLC. MS(ESI+): m/z=440.

Sources & evidence

ORD record
ord-3860d6c21f9248de8bf4239aac7f9a57
Source dataset
uspto-grants-2006_03
Patent number
US07018988B2

Reaction notes

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