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

Sodium ethoxide → HCID 54710119, 화합물

HRID 902482
노트
인쇄 미리보기

반응식

HRID 902482 반응식
[O-]CC.[Na+].CO[C:7]([C:9]1[S:10][CH:11]=[CH:12][C:13]=1[NH:14][C:15](=[O:22])[CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])=[O:8]>C(O)C>[CH2:20]([O:19][C:17]([C:16]1[C:15](=[O:22])[NH:14][C:13]2[CH:12]=[CH:11][S:10][C:9]=2[C:7]=1[OH:8])=[O:18])[CH3:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2723922Sodium ethoxideHCID 2807589HCID 2807589, 화합물

생성물 1

HCID 54710119HCID 54710119, 화합물수율 55%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Sodium ethoxide (0.67 g, 9.29 mmol) was added to a solution of 3-(2-ethoxycarbonyl-acetylamino)-thiophene-2-carboxylic acid methyl ester (1) (2.18 g, 7.74 mmol) in anhydrous ethanol and refluxed overnight. The solution was cooled and excess solvent was distilled off The residue was dissolved in water and acidified by cold diluted HCl solution. The solids formed were filtered, washed by water, and dried under vacuum at room temperature to yield 1.0 g (55%) of 7-hydroxy-5-oxo-4,5-dihydro-thieno[3,2-b]pyridine-6-carboxylic acid ethyl ester as white solid. MP 218° C.; 1H NMR (400 MHz, DMSO-d6) δ 1.28 (t, J=7.2 Hz, 3H), 4.29 (q, J=7.2 Hz, 2H), 6.96 (d, J=5.6 Hz, 1H), 8.07 (d, J=5.6 Hz, 1H) ppm; MS m/z=240 amu (M++1).

후처리

  1. temperaturerefluxed overnight
  2. temperatureThe solution was cooled
  3. distillationexcess solvent was distilled off The residue
  4. dissolutionwas dissolved in water
  5. customThe solids formed
  6. filtrationwere filtered
  7. washwashed by water
  8. customdried under vacuum at room temperature

출처 및 근거

ORD 기록
ord-aceb3aece9f0449bb7f5afea9f0bd064
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07365200B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트