DL-Phenylserine → 2-(2-Tert-butoxycarbonyl-ethyl)-5-phenyl-oxazole-4-carboxylic acid
Reaction equation
[CH:1]1[CH:6]=[CH:5][C:4]([CH:7]([OH:13])[CH:8]([NH2:12])[C:9]([OH:11])=[O:10])=[CH:3][CH:2]=1.[C:14]([O:18][C:19](=[O:25])[CH2:20][CH2:21][C:22](O)=O)([CH3:17])([CH3:16])[CH3:15]>>[C:14]([O:18][C:19]([CH2:20][CH2:21][C:22]1[O:13][C:7]([C:4]2[CH:3]=[CH:2][CH:1]=[CH:6][CH:5]=2)=[C:8]([C:9]([OH:11])=[O:10])[N:12]=1)=[O:25])([CH3:17])([CH3:16])[CH3:15]Participants
3
Procedure
Prepared starting from DL-3-phenylserine hydrate following sequentially general procedures Y, Z with succinic acid mono-tert-butyl ester, Z1 and Z2. LC-MS-conditions 02: tR=0.95 min; [M+H]+=318.32.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-c3b597753f27480398aba6cefc626fba
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08288419B2
Reaction notes
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