(2S)-1-(N-Benzyloxycarbonyl-L-prolyl)-2-[1-hydroxy-2-(phenylsulfinyl)ethyl]pyrrolidine → (2S)-1-(N-benzyloxycarbonyl-L-prolyl)-2-[(phenylsulfinyl)acetyl]-pyrrolidine
Reaction equation
[CH2:1]([O:8][C:9]([N:11]1[CH2:33][CH2:32][CH2:31][C@H:12]1[C:13]([N:15]1[CH2:19][CH2:18][CH2:17][C@H:16]1[CH:20]([OH:30])[CH2:21][S:22]([C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:23])=[O:14])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CS(C)=O.C1CCC(N=C=NC2CCCCC2)CC1>>[CH2:1]([O:8][C:9]([N:11]1[CH2:33][CH2:32][CH2:31][C@H:12]1[C:13]([N:15]1[CH2:19][CH2:18][CH2:17][C@H:16]1[C:20](=[O:30])[CH2:21][S:22]([C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:23])=[O:14])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
(2S)-1-(N-Benzyloxycarbonyl-L-prolyl)-2-[1-hydroxy-2-(phenylsulfinyl)ethyl]pyrrolidine (850 mg) was subjected to DMSO-DCC oxidation as in Example 1-D) to give 672 mg of (2S)-1-(N-benzyloxycarbonyl-L-prolyl)-2-[(phenylsulfinyl)acetyl]-pyrrolidine (See Table 1).
Sources & evidence
- ORD record
- ord-ec50fb5da20f46b0b3a0d750d297158a
- Source dataset
- uspto-grants-1996_04
- Patent number
- US05506256
Reaction notes
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