Benzylamine → HCID 86734605, compound
Reaction equation
C(N)C1C=CC=CC=1.C(OC([NH:19][C@H:20]([C:25]([NH:27][O:28][P:29]([CH3:32])(=[O:31])[OH:30])=[O:26])[CH2:21][CH:22]([CH3:24])[CH3:23])=O)C1C=CC=CC=1>>[NH2:19][C@H:20]([C:25]([NH:27][O:28][P:29]([CH3:32])(=[O:30])[OH:31])=[O:26])[CH2:21][CH:22]([CH3:24])[CH3:23]Participants
3
Procedure
In a manner analogous to Example 1(b), starting from the benzylamine salt of [(N-benzyloxycarbonyl-L-leucyl)amino]-methylphosphonic acid there was obtained (L-leucylamino)-methylphosphonic acid of melting point 262°-264° C (decomposition); [α]D20 = +59.7° (c = 0.67% in water).
Sources & evidence
- ORD record
- ord-b031101d66734b198896517a73e9ab11
- Source dataset
- uspto-grants-1977_04
- Patent number
- US04016148
Reaction notes
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