Veratrylamine → HCID 131725452, 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.[CH3:34][O:35][C:36]1[CH:37]=[C:38]([CH:41]=[CH:42][C:43]=1[O:44][CH3:45])[CH2:39][NH2:40]>>[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:40][CH2:39][C:38]2[CH:41]=[CH:42][C:43]([O:44][CH3:45])=[C:36]([O:35][CH3:34])[CH:37]=2)=[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 3,4-dimethoxybenzylamine the title compound was obtained in 58% purity by LC/MS. MS(ESI+): m/z=488.4.
Sources & evidence
- ORD record
- ord-839e53a390914275aa0e043449ff5335
- Source dataset
- uspto-grants-2006_03
- Patent number
- US07018988B2
Reaction notes
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