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tert-Butoxy bis(dimethylamino)methane → 2-[2-(Dimethylamino)ethenyl]-1,6-dihydro-6-oxo-3-pyridinecarbonitrile

HRID 542511
ノート
印刷プレビュー

反応式

HRID 542511 の反応式
[CH3:1][C:2]1[NH:3][C:4](=[O:10])[CH:5]=[CH:6][C:7]=1[C:8]#[N:9].[CH3:11][N:12]([CH:14](N(C)C)OC(C)(C)C)[CH3:13]>CN(C)C=O>[CH3:11][N:12]([CH3:14])[CH:13]=[CH:1][C:2]1[NH:3][C:4](=[O:10])[CH:5]=[CH:6][C:7]=1[C:8]#[N:9]
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

4

反応物 2

HCID 79885tert-Butoxy bis(dimethylamino)methane2 回HCID 113785166-Hydroxy-2-methylnicotinonitrile

生成物 1

HCID 544759082-[2-(Dimethylamino)ethenyl]-1,6-dihydro-6-oxo-3-pyridinecarbonitrile

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
110 °C

実験手順

To a stirred mixture containing 6.7 g of 1,6-dihydro-2-methyl-6-oxo-3-pyridinecarbonitrile in 100 ml of dimethylformamide was quickly added 11.5 ml of bis(dimethylamino)-t-butoxymethane and the reaction mixture was heated with stirring for 3 hours at 110° C. After a tlc analysis had shown some of the starting material still present, another 2.3 ml of bis(dimethylamino)-t-butoxymethane was added, the reaction mixture was heated with stirring to reflux for 90 minutes, and then allowed to cool to room temperature and stand overnight. The mixture was chilled and the separated product was collected, washed with chilled ethanol and dried in a vacuum oven at 90° C. to yield 8.2 g of 2-[2-(dimethylamino)ethenyl]-1,6-dihydro-6-oxo-3-pyridinecarbonitrile, m.p. 298°-300° C.

後処理

  1. temperaturethe reaction mixture was heated
  2. temperaturethe reaction mixture was heated
  3. stirringwith stirring
  4. temperatureto reflux for 90 minutes
  5. temperatureto cool to room temperature
  6. waitstand overnight
  7. temperatureThe mixture was chilled
  8. customthe separated product was collected
  9. washwashed with chilled ethanol
  10. customdried in a vacuum oven at 90° C.

出典と根拠

ORDレコード
ord-6c5d6854b5854fbe846e2873d1371972
出典データセット
uspto-grants-1987_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04657915

反応ノート

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