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

HRID 902502
Notes
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Reaction equation

HRID 902502 reaction equation
[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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 2723922Sodium ethoxideHCID 5178717HCID 5178717, compound

Product 1

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

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

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).

Workup

  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

Sources & evidence

ORD record
ord-c3f3b3c656fb47c697595c3e5ecb1d3e
Source dataset
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07365200B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes