Lithium Hydroxide → 5-(4-tert-Butylphenyl)-4-(phenylsulfonyl)pyrrolidine-2-carboxylic Acid
Reaction equation
C([O:3][C:4]([CH:6]1[CH2:10][CH:9]([S:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)(=[O:13])=[O:12])[CH:8]([C:20]2[CH:25]=[CH:24][C:23]([C:26]([CH3:29])([CH3:28])[CH3:27])=[CH:22][CH:21]=2)[NH:7]1)=[O:5])C.[OH-].[Li+]>>[C:26]([C:23]1[CH:22]=[CH:21][C:20]([CH:8]2[NH:7][CH:6]([C:4]([OH:5])=[O:3])[CH2:10][CH:9]2[S:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)(=[O:13])=[O:12])=[CH:25][CH:24]=1)([CH3:29])([CH3:27])[CH3:28]Participants
3
Procedure
In analogy to the procedure described in example 253e, 5-(4-tert-butylphenyl)-4-(phenylsulfonyl)pyrrolidine-2-carboxylic acid ethyl ester was saponified in the presence of lithium hydroxide to give the title compound as colorless solid which was used in the next step without further purification. MS (ESI): m/z=388.2 [M+H]
Sources & evidence
- ORD record
- ord-14433362cc5e446a88da13f7ddbbfb03
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08163793B2
Reaction notes
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