反応 #348500

ord-a6ac13c602844c159491d47fe00fb0a2

反応方程式

O=C(O)C[C@H](NC(=O)OCc1ccccc1)C(=O)O
N-benzyloxycarbonyl-L-aspartic acid
COC(=O)[C@@H](N)Cc1ccccc1
L-phenylalanine methyl ester
COC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(=O)O)NC(=O)OCc1ccccc1
N-benzyloxycarbonyl-L-aspartyl-L-phenylalanine methyl ester
COC(=O)[C@@H](N)Cc1ccccc1
L-phenylalanine methyl ester
収率 95.5%

反応条件

温度
38°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The precipitate was collected
  2. 2
    洗浄washed with water
  3. 3
    その他dried

実験手順

A 267.2 mg (1 m mol) of N-benzyloxycarbonyl-L-aspartic acid and 537.6 mg (3 m mol) of L-phenylalanine methyl ester were dissolved in 5 ml of McIlvain's buffer solution (pH:7.0). The resulting solution was admixed with 100 mg of Thermoase and 100 mg of potato inhibitor and shaken at 38° C. for 20 hours. The precipitate was collected and washed with water and dried to obtain 580 mg of a crude crystalline addition compound of N-benzyloxycarbonyl-L-aspartyl-L-phenylalanine methyl ester and L-phenylalanine methyl ester (1:1) (melting point: 123 to 125° C.; Yield: 95.5 % based on N-benzyloxycarbonyl-L-aspartic acid).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04165311uspto-grants-1979_08