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

Sodium Carbonate → HCID 10636627, 화합물

HRID 1241695
노트
인쇄 미리보기

반응식

HRID 1241695 반응식
CC(C)(C)C(NC1C=CC=CC=1[C:12]1[C:25]2[C:24](=O)[C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[N:17]([CH3:27])[C:16]=2[CH:15]=[CH:14][CH:13]=1)=O.C([O-])([O-])=O.[Na+].[Na+]>C1COCC1>[CH3:27][N:17]1[C:16]2[C:25]3[C:12](=[C:15]4[C:16](=[N:17][C:24]=3[C:23]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]1=3)[CH:25]=[CH:12][CH:13]=[CH:14]4)[CH:13]=[CH:14][CH:15]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10340Sodium CarbonateHCID 10927115HCID 10927115, 화합물2회

생성물 1

HCID 10636627HCID 10636627, 화합물수율 95%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

(Method H-2) (Cyclisation) 2,2-Dimethyl-N-[2-(10-methyl-9-oxo-9,10-dihydro-acridin-1-yl)-phenyl]-propionamide, 25 (50 mg, 0.13 mmol) was dissolved in 1:1 THF/6N HCl (20 mL) and the mixture heated to reflux for 5 days giving a bright orange solution. The mixture was basified (aq. Na2CO3) and extracted with ethyl acetate (50 mL) and the organic layer dried (Na2SO4), and evaporated under reduced pressure. The crude product was purified by column chromatography (1:4 EtOAc: hexane) to give the title compound as a yellow solid (35 mg, 0.12 mmol, 95%).

후처리

  1. temperaturethe mixture heated
  2. temperatureto reflux for 5 days
  3. customgiving a bright orange solution
  4. extractionextracted with ethyl acetate (50 mL)
  5. dry with materialthe organic layer dried (Na2SO4)
  6. customevaporated under reduced pressure
  7. customThe crude product was purified by column chromatography (1:4 EtOAc: hexane)

출처 및 근거

ORD 기록
ord-92a1c5a23df047dd8f818f00490c16ed
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07115619B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트