Phosphorus trichloride → N-acetoacetyl-L-aspartyl-L-phenylalanine methyl ester

HRID 325270ノート

反応式

HRID 325270 の反応式
[C:1]([NH:7][C@H:8]([C:13]([O-:15])=O)[CH2:9][C:10]([O-:12])=[O:11])(=[O:6])[CH2:2][C:3]([CH3:5])=[O:4].[Na+].[Na+].P(Cl)(Cl)Cl.C(N[C@@H]1C(=O)OC(=O)C1)(=O)CC(C)=O.[CH3:36][O:37][C:38](=[O:48])[C@H:39]([CH2:41][C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1)[NH2:40]>O1CCOCC1.C(O)(=O)C.C(OCC)(=O)C>[CH3:36][O:37][C:38](=[O:48])[C@H:39]([CH2:41][C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1)[NH:40][C:13](=[O:15])[C@H:8]([CH2:9][C:10](=[O:11])[OH:12])[NH:7][C:1](=[O:6])[CH2:2][C:3]([CH3:5])=[O:4]

参加物

8

実験手順

Crude disodium N-acetoacetylaspartate, 28.51 parts, was stirred with 200 parts by volume of ethyl acetate and 11.7 parts by volume of acetic acid at 0°-5° C. under argon while 4.37 parts by volume of phosphorous trichloride was added dropwise. The resulting mixture was allowed to warm to ambient temperatures while stirring for 20 hours. To the resulting solution which contains N-acetoacetyl-L-aspartic anhydride was added dropwise over a 2 hour period 122 parts by volume of 0.9 M L-phenylalanine methyl ester in dioxane. After continued stirring for 20 hours, the solvent was evaporated under vacuum at 35°-40° C. Toluene, 200 parts by volume, was added to the residue and the evaporation was repeated, giving crude N-acetoacetyl-L-aspartyl-L-phenylalanine methyl ester as a semi-solid yellow residue.

後処理

  1. additionwas added dropwise
  2. temperatureto warm to ambient temperatures
  3. stirringAfter continued stirring for 20 hours
  4. customthe solvent was evaporated under vacuum at 35°-40° C
  5. additionToluene, 200 parts by volume, was added to the residue
  6. customthe evaporation

出典と根拠

ORDレコード
ord-ae02da52df18469f80af1069646dabb4
出典データセット
uspto-grants-1984_04
特許番号
US04440677

反応ノート

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