홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Trimethyl orthoformate → 7-Methoxycarbonylmethyl-2-(4-(4-phenylbenzoylamino)butyl)-1,2,3,4-tetrahydroisoquinoline

HRID 1003711
노트
인쇄 미리보기

반응식

HRID 1003711 반응식
O.O.O.[N+]([O-])([O-])=O.[Tl+3].[N+]([O-])([O-])=O.[N+]([O-])([O-])=O.[CH:17]([O:22][CH3:23])([O:20]C)OC.Cl.[C:25]([C:28]1[CH:37]=[C:36]2[C:31]([CH2:32][CH2:33][N:34]([CH2:38][CH2:39][CH2:40][CH2:41][NH:42][C:43](=[O:56])[C:44]3[CH:49]=[CH:48][C:47]([C:50]4[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=4)=[CH:46][CH:45]=3)[CH2:35]2)=[CH:30][CH:29]=1)(=O)C>CO.ClCCl>[CH3:23][O:22][C:17]([CH2:25][C:28]1[CH:37]=[C:36]2[C:31]([CH2:32][CH2:33][N:34]([CH2:38][CH2:39][CH2:40][CH2:41][NH:42][C:43](=[O:56])[C:44]3[CH:45]=[CH:46][C:47]([C:50]4[CH:51]=[CH:52][CH:53]=[CH:54][CH:55]=4)=[CH:48][CH:49]=3)[CH2:35]2)=[CH:30][CH:29]=1)=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 9005Trimethyl orthoformateHCID 11270721Nitric acid,thallium(3+) salt, trihydrate (9CI)HCID 1317217547-Acetyl-2-(4-(4-phenylbenzoylamino)butyl)-1,2,3,4-tetrahydroisoquinoline, hydrochloride

생성물 1

HCID 187970057-Methoxycarbonylmethyl-2-(4-(4-phenylbenzoylamino)butyl)-1,2,3,4-tetrahydroisoquinoline수율 30%

시약·촉매·용매 2

HCID 887
Methanol
용매
HCID 6344Dichloromethane용매

실험 절차

A mixture of thallium (III) nitrate trihydrate (0.73 g, 1.6 mmol), K10 clay (1.65 g) and trimethyl orthoformate (1.8 ml, 1.6 mmol) in methanol (3 ml) was stirred at room temperature for 15 min. The solvent was evaporated in vacuo and dichloromethane (5 ml) was added to the residue. To this mixture was added a solution of 7-acetyl-2-(4-(4-phenylbenzoylamino)butyl)-1,2,3,4-tetrahydroisoquinoline, hydrochloride (0.50 g, 1.1 mmol) in dichloromethane (15 ml) and the reaction mixture was stirred for 4 h. The suspended solid was removed by filtration and the filtrate was washed with saturated aqueous potassium carbonate (2×30 ml), then brine (30 ml). Drying (Na2SO4) and evaporation in vacuo afforded a yellow gum which was chromatographed on silica using 20-100% ethyl acetate--pentane gradient elution to afford the title compound as an off-white solid (0.15 g, 30%).

후처리

  1. customThe solvent was evaporated in vacuo and dichloromethane (5 ml)
  2. additionwas added to the residue
  3. customThe suspended solid was removed by filtration
  4. washthe filtrate was washed with saturated aqueous potassium carbonate (2×30 ml)
  5. customDrying
  6. custom(Na2SO4) and evaporation in vacuo
  7. customafforded a yellow gum which
  8. customwas chromatographed on silica using 20-100% ethyl acetate
  9. washpentane gradient elution

출처 및 근거

ORD 기록
ord-541ee847a9484995948dd89a307411f6
출처 데이터셋
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06046210

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트