(S)-(-)-1-Benzyl-3-pyrrolidinol → HCID 86583596, compound
Reaction equation
[CH2:1]([N:8]1[CH2:12][CH2:11][C@H:10]([OH:13])[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1(C)C(S(C2C=CC(CN3CC[C@H](O)C3)=CC=2)(=O)=O)=CC=CC=1.[S:37]([C:41]1[CH:47]=[CH:46][C:44]([CH3:45])=[CH:43][CH:42]=1)([O-:40])(=[O:39])=[O:38]>>[CH2:1]([N:8]1[CH2:12][CH2:11][C@H:10]([OH:13])[CH2:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1.[S:37]([C:41]1[CH:47]=[CH:46][C:44]([CH3:45])=[CH:43][CH:42]=1)([O-:40])(=[O:39])=[O:38]Participants
3
Procedure
This was prepared from (S)-1-benzyl-3-pyrrolidinol and p-toluenesulfonyl (S)-1-Benzyl-3-pyrrolidinol-tosylate Preparation 24.
Sources & evidence
- ORD record
- ord-a1b99ed612054258ba8503acc6aa3349
- Source dataset
- uspto-grants-2001_09
- Patent number
- US06294557B1
Reaction notes
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