Serinol → HCID 131725620, compound
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.[C:19]1([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[CH:24]=[CH:23][C:22](C(Cl)=O)=[CH:21][CH:20]=1.[NH2:34][CH:35]([CH2:38][OH:39])[CH2:36][OH:37]>>[C:28]1([C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)[CH:29]=[CH:30][C:31]([C:6]([N:8]2[CH2:12][C:11](=[N:13][O:14][CH3:15])[CH2:10][C@H:9]2[C:16]([NH:34][CH:35]([CH2:38][OH:39])[CH2:36][OH:37])=[O:18])=[O:7])=[CH:32][CH:33]=1Participants
4
Procedure
Following the general method as outlined in Example 22, starting from (2S,4EZ)-1-(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidinecarboxylic acid, [1,1′-biphenyl]-4-carbonyl chloride, and 2-amino-1,3-propanediol, the title compound was obtained in 61% purity by HPLC. MS(ESI+): m/z=412.
Sources & evidence
- ORD record
- ord-634c8afb9b954f049a10e4af896f9d41
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07211601B2
Reaction notes
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