Toluene → L-aspartyl-L-phenylalanine methyl ester hydrochloride dihydrate

HRID 1583897

반응식

HRID 1583897 반응식
[CH3:1][O:2][C:3](=[O:27])[C@H:4]([CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[NH:5][C:6](=[O:19])[C@H:7]([CH2:15][C:16](=[O:18])[OH:17])[NH:8]C(=O)CC(C)=O.C1(C)C=CC=CC=1.[ClH:35].N[OH:37]>O.C(O)(=O)C>[OH2:2].[OH2:37].[ClH:35].[CH3:1][O:2][C:3](=[O:27])[C@H:4]([CH2:20][C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1)[NH:5][C:6](=[O:19])[C@H:7]([CH2:15][C:16](=[O:17])[OH:18])[NH2:8]

참가 물질

6

실험 절차

The crude N-acetoacetyl-L-aspartyl-L-phenylalanine methyl ester was dissolved in 100 parts by volume of water and 11.7 parts by volume of acetic acid. Toluene, 200 parts by volume, and hydroxylamine hydrochloride, 6.95 parts by volume, were added and the mixture stirred for 2.5 hours. The aqueous layer was separated and cooled to 0°-5° C. 15 parts by volume concentrated hydrochloric acid were added and the resulting mixture was cooled at 0°-5° C. overnight. The precipitate was collected on a filter and air dried for 3 hours to give 26.4 parts of α-L-aspartyl-L-phenylalanine methyl ester hydrochloride dihydrate.

후처리

  1. customThe aqueous layer was separated
  2. temperaturecooled to 0°-5° C
  3. addition15 parts by volume concentrated hydrochloric acid were added
  4. temperaturethe resulting mixture was cooled at 0°-5° C. overnight
  5. customThe precipitate was collected on
  6. filtrationa filter
  7. customair dried for 3 hours

출처 및 근거

ORD 기록
ord-f3e3adb7087f4835af9484840d256308
출처 데이터셋
uspto-grants-1985_11
특허 번호
US04555362

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