N-Benzyloxycarbonyl-beta-alanine → Ethyl 5-benzyloxycarbonylamino-3-oxo-pentanoate
Reaction equation
[C:1]([NH:11][CH2:12][CH2:13][C:14]([OH:16])=O)([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:2].O=C(C1C=CC=CN=1)[CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21]>>[CH2:4]([O:3][C:1]([NH:11][CH2:12][CH2:13][C:14](=[O:16])[CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21])=[O:2])[C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1Participants
3
Procedure
Ethyl 5-benzyloxycarbonylamino-3-oxo-pentanoate was prepared from N-Cbz-β-alanine in the same manner as ethyl 3-oxo-3-pyridin-2-yl-propionate (Example 94).
Sources & evidence
- ORD record
- ord-65c593e46deb4d9dbd945bbfee6b7ad5
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07214802B2
Reaction notes
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