Nicotinic Acid → 2-Benzoyl amino-pentane dioic acid dimethyl ester

HRID 82482노트

반응식

HRID 82482 반응식
[CH:1]1[CH:6]=N[CH:4]=[C:3]([C:7]([OH:9])=O)[CH:2]=1.[CH3:10]N1CCOCC1.CCN=C=NCCCN(C)C.Cl.[CH3:29][O:30][C:31](=[O:40])[C@H:32]([CH2:34][CH2:35][C:36]([O:38][CH3:39])=[O:37])[NH2:33]>C(Cl)Cl>[CH3:29][O:30][C:31](=[O:40])[C:32]([NH2:33])([C:7](=[O:9])[C:3]1[CH:2]=[CH:1][CH:6]=[CH:10][CH:4]=1)[CH2:34][CH2:35][C:36]([O:38][CH3:39])=[O:37]

참가 물질

6

반응 조건

온도
25 °C

실험 절차

To a solution of niacin (1.4 g, 11.42 mmol) in DCM (20 mL) were added N-methyl morpholine (3.76 mL, 34.2 mmol), EDCI.HCl (4.36 g, 34.2 mmol) and L-glutamic acid dimethyl ester (2.0 g, 11.42 mmol). The mixture was allowed to stir at room temperature (25° C.) over 3 h under nitrogen atmosphere. The resulting mixture was diluted with DCM (100 mL), washed with water (3×50 mL) and dried over sodium sulphate. The crude product obtained upon evaporation of the solvent was further purified by silica gel column chromatography to obtain required product as pale yellow oil (3.1 g, 73%).

후처리

  1. washwashed with water (3×50 mL)
  2. dry with materialdried over sodium sulphate
  3. customThe crude product obtained upon evaporation of the solvent
  4. customwas further purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-466ad572ab5643d8b303080aa2f9a680
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08846721B2

반응 노트

불러오는 중…