Benzylamine → Alafosfalin

HRID 866633Notes

Reaction equation

HRID 866633 reaction equation
C(N)C1C=CC=CC=1.C(OC([NH:19][C@H:20]([C:22]([NH:24][C@H:25]([P:27](=[O:30])([OH:29])[OH:28])[CH3:26])=[O:23])[CH3:21])=O)C1C=CC=CC=1>>[NH2:19][C@H:20]([C:22]([NH:24][C@H:25]([P:27](=[O:28])([OH:30])[OH:29])[CH3:26])=[O:23])[CH3:21]

Participants

3

Reactant 2

HCID 7504BenzylamineHCID 13002188HCID 13002188, compound

Product 1

HCID 71957Alafosfalin

Procedure

In a manner analogous to that described in the last paragraph of Example A, starting from the benzylamine salt of (1R)-1-[(N-benzyloxycarbonyl-L-alanyl)amino]-ethylphosphonic acid there was obtained (1R)-1-(L-alanylamino)-ethylphosphonic acid of melting point 295°-296° C (decomposition); [α]D20 = -45.6° (c = 1% in water).

Sources & evidence

ORD record
ord-919c8c4fc6f4486f8446f8950a4637d0
Source dataset
uspto-grants-1978_07
Patent number
US04100275

Reaction notes

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