(S)-4-[2-((S)-4-hydroxy-6-aza-spiro[2.5]oct-6-yl)-ethyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester → [(S)-3-((S)-4-Hydroxy-6-aza-spiro[2.5]oct-6-yl)-1-hydroxymethyl-propyl]-carbamic acid benzyl ester
Reaction equation
[CH2:1]([O:8][C:9]([N:11]1[C@@H:15]([CH2:16][CH2:17][N:18]2[CH2:25][CH2:24][C:21]3([CH2:23][CH2:22]3)[C@H:20]([OH:26])[CH2:19]2)[CH2:14][O:13]C1(C)C)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>CO.O>[CH2:1]([O:8][C:9](=[O:10])[NH:11][C@H:15]([CH2:14][OH:13])[CH2:16][CH2:17][N:18]1[CH2:25][CH2:24][C:21]2([CH2:23][CH2:22]2)[C@H:20]([OH:26])[CH2:19]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of (S)-4-[2-((S)-4-hydroxy-6-aza-spiro[2.5]oct-6-yl)-ethyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester (5.00 g, 12.9 mmol) in methanol/water 9:1 (50 mL) was stirred at room temperature in the presence of Amberlite® IR-120 resin (15.8 g). After 16 h the resin was collected by filtration and washed with methanol. The filtrate was discarded, and the product was recovered by digesting the Amberlite® resin three times in 7 M methanolic ammonia solution (60 mL) at room temperature over 15 min. The ammonia solutions were combined and evaporated to afford the title compound (4.27 g, 95%). Colorless oil, MS (ISP)=349.3 (M+H)+.
Workup
- filtrationAfter 16 h the resin was collected by filtration
- washwashed with methanol
- customthe product was recovered
- customat room temperature
- customover 15 min
- customevaporated
Sources & evidence
- ORD record
- ord-f5955bb97c7e41759949d416fb940bdf
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08071586B2
Reaction notes
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