4-Phenylbenzoyl chloride → HCID 58714550, 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.O[NH:35][C:36](=[NH:42])[CH2:37][S:38]([CH3:41])(=[O:40])=[O:39]>>[CH3:15][O:14][N:13]=[C:11]1[CH2:10][C@@H:9]([C:16]2[O:18][N:42]=[C:36]([CH2:37][S:38]([CH3:41])(=[O:40])=[O:39])[N:35]=2)[N:8]([C:6]([C:31]2[CH:30]=[CH:29][C:28]([C:19]3[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=3)=[CH:33][CH:32]=2)=[O:7])[CH2:12]1Participants
4
Procedure
Following the general method as outlined in Example 59, starting from (2S,4EZ)-1-(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidine-carboxylic acid (Intermediate 2), [1,1′-biphenyl]-4-carbonyl chloride, and N-hydroxy-2-(methylsulfonyl)ethanimidamide, the title compound was obtained in 87% purity by HPLC. MS(ESI+): m/z=455.2.
Sources & evidence
- ORD record
- ord-1e5972e274d14168a64ec1621c2a745c
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07115639B2
Reaction notes
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