Benzyl 3-aminopropanoate → HCID 19037105, compound
Reaction equation
[O:1]=[C:2]([NH:22][CH2:23][CH2:24][C:25]([O:27][CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)=[O:26])/[C:3](/[CH2:17][S:18][C:19](=[O:21])[CH3:20])=[CH:4]/[C:5]1C=C[C:8]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:7][CH:6]=1.NCCC(OCC1C=CC=CC=1)=O>>[O:1]=[C:2]([NH:22][CH2:23][CH2:24][C:25]([O:27][CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)=[O:26])/[C:3](/[CH2:17][S:18][C:19](=[O:21])[CH3:20])=[CH:4]/[C:5]1[C:12]2[C:11](=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:8]=[CH:7][CH:6]=1Participants
3
Procedure
The above (Z) acid is coupled with benzyl β-alaninate according to the experimental procedure described in Example 1 (step D).
Sources & evidence
- ORD record
- ord-28867bde5a3d414bb06361308e9196b7
- Source dataset
- uspto-grants-1997_07
- Patent number
- US05646313
Reaction notes
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