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Sodium ethoxide → 7-Hydroxy-5-oxo-4,5-dihydro-thieno[3,2-b]pyridine-6-carbonitrile

HRID 902502
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HRID 902502 반응식
[O-]CC.[Na+].CO[C:7]([C:9]1[S:10][CH:11]=[CH:12][C:13]=1[NH:14][C:15](=[O:19])[CH2:16][C:17]#[N:18])=[O:8]>C(O)C>[OH:8][C:7]1[C:9]2[S:10][CH:11]=[CH:12][C:13]=2[NH:14][C:15](=[O:19])[C:16]=1[C:17]#[N:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2723922Sodium ethoxideHCID 5178717HCID 5178717, 화합물

생성물 1

HCID 546791707-Hydroxy-5-oxo-4,5-dihydro-thieno[3,2-b]pyridine-6-carbonitrile수율 84%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Sodium ethoxide (3.10 g, 45.62 mmol) was added to a solution of 3-(2-cyano-acetylamino)-thiophene-2-carboxylic acid methyl ester (24) (3.10 g, 45.62 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 to pH 2 by cold diluted HCl solution. The solids formed were filtered, washed by cold water, and dried under vacuum at room temperature to yield 6.7 g (84%) of 7-hydroxy-5-oxo-4,5-dihydro-thieno[3,2-b]pyrdine-6-carbonitrile as white solids. MP>300° C.; 1H NMR (400 MHz, DMSO-d6) δ 6.96 (d, J=5.2 Hz, 1H), 8.04 (d, J=5.2 Hz, 1H), 12.10 (s, 1H) ppm; MS mz=193 amu(M++1).

후처리

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

출처 및 근거

ORD 기록
ord-c3f3b3c656fb47c697595c3e5ecb1d3e
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07365200B2

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