3-Amino-1-propanol → HCID 131725602, compound
Reaction equation
C(OC([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)(C)(C)C.[C:19]1([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[CH:24]=[CH:23][C:22]([S:25](Cl)(=[O:27])=[O:26])=[CH:21][CH:20]=1.[NH2:35][CH2:36][CH2:37][CH2:38][OH:39]>>[C:19]1([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[CH:24]=[CH:23][C:22]([S:25]([N:8]2[CH2:12][C:11](=[N:13][O:14][CH3:15])[CH2:10][C@H:9]2[C:16]([NH:35][CH2:36][CH2:37][CH2:38][OH:39])=[O:18])(=[O:27])=[O:26])=[CH:21][CH:20]=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-sulfonyl chloride, and 3-amino-1-propanol, the title compound was obtained in 64% purity by HPLC. MS(ESI+): m/z=432.
Sources & evidence
- ORD record
- ord-613c6ecbaadc4149805d5d17149e0343
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07211601B2
Reaction notes
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