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Diethyl Ether → 4-Ethenyl-6-(methyloxy)-1,5-naphthyridine-3-carbonitrile

HRID 638978
Notes
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Reaction equation

HRID 638978 reaction equation
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([O:12][CH3:13])[N:10]=2)[N:5]=[CH:4][C:3]=1[C:14]#[N:15].C(=O)([O-])[O-].[K+].[K+].[CH2:22](OCC)[CH3:23]>COCCOC.O>[CH:22]([C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([O:12][CH3:13])[N:10]=2)[N:5]=[CH:4][C:3]=1[C:14]#[N:15])=[CH2:23]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 3283Diethyl Ether2×HCID 11430Potassium CarbonateHCID 685791014-Chloro-6-methoxy-1,5-naphthyridine-3-carbonitrile

Product 1

HCID 592543544-Ethenyl-6-(methyloxy)-1,5-naphthyridine-3-carbonitrileYield 65%

Reagents, catalysts & solvents 1

HCID 18180031Water 1,2-dimethoxyethaneSolvent

Conditions

Temperature
90 °C

Procedure

To a solution of 4-chloro-6-(methyloxy)-1,5-naphthyridine-3-carbonitrile (280 mg, 1.28 mmol), potassium carbonate (885 mg, 6.4 mmole), tetrakis-triphenylphosphine (30 mg, 0.026 mmole) in DME/H2O (20 mL, 3:1) was added 2,4,6-trivinylcycloborane-pyridine complex (154 mg, 0.64 mmole). After stirring for 1 h at 90° C., another batch of tetrakis-triphenylphosphine (30 mg, 0.026 mmol) was added. After refluxing for another 1.5 h, the mixture contents were cooled down to room temperature and extrated with diethyl ether. The ether fractions were combined, concentrated and purified by column chromatography (silica, 0-10% ethyl acetate in hexane) to give the title compound as a light yellow solid (176 mg, 65%): LC/MS (ES) m/e 212 (M+H)+.

Workup

  1. temperatureAfter refluxing for another 1.5 h
  2. temperaturethe mixture contents were cooled down to room temperature
  3. concentrationconcentrated
  4. custompurified by column chromatography (silica, 0-10% ethyl acetate in hexane)

Sources & evidence

ORD record
ord-9167a1cdaa2a497ba0125f0f4de0cd77
Source dataset
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07691850B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes