Benzylamine → HCID 54358335, compound
Reaction equation
[CH2:1](N)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(OC([NH:19][C@H:20]([C:22]([NH:24][C@H:25]([P:27](=[O:30])([OH:29])[OH:28])C)=[O:23])[CH3:21])=O)C1C=CC=CC=1>CO>[NH2:19][C@H:20]([C:22]([NH:24][C@H:25]([P:27](=[O:28])([OH:30])[OH:29])[CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)=[O:23])[CH3:21]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In a manner analogous to that given in Example 1 (b) but with ion-exchange in methanol, from the benzylamine salt of (1R)-1-[(N-benzyloxycarbonyl-L-alanyl)amino]-ethylphosphonic acid there was obtained (1R)-1-(L-alanylamino)-2-phenylethylphosphonic acid of melting point 250°-260° C (decomposition); [α]D20 = -40.3° (c = 0.21% in water).
Sources & evidence
- ORD record
- ord-661646a7756d45baaa5a4915a3f72838
- Source dataset
- uspto-grants-1977_04
- Patent number
- US04016148
Reaction notes
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