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

HRID 638978
ノート
印刷プレビュー

反応式

HRID 638978 の反応式
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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 18180031Water 1,2-dimethoxyethane溶媒

反応条件

温度
90 °C

実験手順

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)+.

後処理

  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)

出典と根拠

ORDレコード
ord-9167a1cdaa2a497ba0125f0f4de0cd77
出典データセット
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07691850B2

反応ノート

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