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Sodium ethoxide → 1,6-Naphthyridin-2(1H)-one, 5,8-dimethyl-

HRID 868981
Notes
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Reaction equation

HRID 868981 reaction equation
[NH2:1][C:2]1[C:7]([CH3:8])=[CH:6][N:5]=[C:4]([CH3:9])[C:3]=1/[CH:10]=[CH:11]/[C:12]([O:14]CC)=O.C([O-])C.[Na+]>C(O)C>[CH3:9][C:4]1[N:5]=[CH:6][C:7]([CH3:8])=[C:2]2[C:3]=1[CH:10]=[CH:11][C:12](=[O:14])[NH:1]2
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 2723922Sodium ethoxideHCID 70648563HCID 70648563, compound

Product 1

HCID 701163661,6-Naphthyridin-2(1H)-one, 5,8-dimethyl-Yield 58.2%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
80 °C

Procedure

A mixture of (E)-ethyl 3-(4-amino-2,5-dimethylpyridin-3-yl)acrylate (5 g, 22.7 mmol) and sodium ethanolate (6.2 g, 91 mmol) in ethanol (100 mL) was heated to 80° C. for 2 h. The reaction mixture was concentrated and diluted with water (50 mL). The aqueous phase was extracted with EtOAc (100 mL×3), and the combined organic layers were washed with saturated sodium chloride solution, dried with sodium sulfate, and concentrated to give 2.3 g of the product as a yellow solid. MS (ESI): m/z 175.1 [M+H]+.

Workup

  1. concentrationThe reaction mixture was concentrated
  2. additiondiluted with water (50 mL)
  3. extractionThe aqueous phase was extracted with EtOAc (100 mL×3)
  4. washthe combined organic layers were washed with saturated sodium chloride solution
  5. dry with materialdried with sodium sulfate
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-9a749d6ff6294f38877a5ad4a12e0ff9
Source dataset
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08969349B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes