Dichloromethane → HCID 67345002, 화합물

HRID 2036879노트

반응식

HRID 2036879 반응식
Cl.[CH2:2]1[C:11]2[C:6](=[CH:7][C:8]([C:12]([O:14][CH3:15])=[O:13])=[CH:9][CH:10]=2)[CH2:5][CH2:4][NH:3]1.C(N(CC)CC)C.ClCCl.Cl[C:27]([O:29][CH2:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)=[O:28]>CN(C1C=CN=CC=1)C.O>[CH2:2]1[C:11]2[C:6](=[CH:7][C:8]([C:12]([O:14][CH3:15])=[O:13])=[CH:9][CH:10]=2)[CH2:5][CH2:4][N:3]1[C:27]([O:29][CH2:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)=[O:28]

참가 물질

7

반응 조건

온도
0 °C

실험 절차

A mixture of 10 g methyl 1,2,3,4-tetrahydroisoquinoline-6-carboxylate hydrochloride, 10 ml triethylamine, and 15 ml dichloromethane with 525 mg DMAP is stirred at 0° C. and 9.3 ml of benzyl chloroformate are added dropwise. After stirring overnight at ambient temperature, the reaction mixture is added to cold water. The organic phase is washed, dried, and evaporated. The crude product is purified by a silica gel chromatography.

후처리

  1. stirringAfter stirring overnight at ambient temperature
  2. washThe organic phase is washed
  3. customdried
  4. customevaporated
  5. customThe crude product is purified by a silica gel chromatography

출처 및 근거

ORD 기록
ord-a6f8ec461b1c474186b1886233d3c357
출처 데이터셋
uspto-grants-2013_11
특허 번호
US08575193B2

반응 노트

불러오는 중…