Triethylamine → N-(t-butoxycarbonyl)-3-phenoxy-DL-phenylalanine 4-pyridylamide

HRID 2351825노트

반응식

HRID 2351825 반응식
[C:1]([O:5][C:6]([NH:8][CH:9]([C:24](O)=[O:25])[CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([O:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH:12]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C(N(CC)CC)C.C(Cl)(=O)OCC.[NH2:40][C:41]1[CH:46]=[CH:45][N:44]=[C:43](Cl)[CH:42]=1>O1CCCC1>[N:44]1[CH:45]=[CH:46][C:41]([NH:40][C:24](=[O:25])[CH:9]([CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([O:17][C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[CH:12]=2)[NH:8][C:6]([O:5][C:1]([CH3:4])([CH3:2])[CH3:3])=[O:7])=[CH:42][CH:43]=1

참가 물질

6

실험 절차

N-(t-butoxycarbonyl)-3-phenoxy-DL-phenylalanine (4.40 g) was dissolved in dry tetrahydrofuran (100 ml) and triethylamine (1.80 ml) was added under ice-cooling, followed by stirring for 15 minutes. To this solution was added ethyl chlorocarbonate (1.44 g) and the mixture was stirred for 30 minutes. After adding 4-amino-2-chloropyridine (1.54 g), the reaction was carried out at room temperature for 10 hours. Thereafter, the solid was filtered off and the filtrate was concentrated under a reduced pressure. The residue was extracted with ethyl acetate. The extract was purified with a column chromatography (hexane/ethyl acetate=3/1) to obtain N-(t-butoxycarbonyl)-3-phenoxy-DL-phenylalanine 4-(2-chloro)pyridylamide (I) (0.60 g), which was confirmed by the following NMR analysis, in the form of a white powder.

후처리

  1. temperaturecooling
  2. stirringthe mixture was stirred for 30 minutes
  3. waitthe reaction was carried out at room temperature for 10 hours
  4. filtrationThereafter, the solid was filtered off
  5. concentrationthe filtrate was concentrated under a reduced pressure
  6. extractionThe residue was extracted with ethyl acetate
  7. customThe extract was purified with a column chromatography (hexane/ethyl acetate=3/1)

출처 및 근거

ORD 기록
ord-779bc097ce03442985ad099aa1df2136
출처 데이터셋
uspto-grants-1989_10
특허 번호
US04873253

반응 노트

불러오는 중…