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

HRID 542511
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HRID 542511 반응식
[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]
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참가 물질

4

반응물 2

HCID 79885tert-Butoxy bis(dimethylamino)methane2회HCID 113785166-Hydroxy-2-methylnicotinonitrile

생성물 1

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

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
110 °C

실험 절차

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.

후처리

  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.

출처 및 근거

ORD 기록
ord-6c5d6854b5854fbe846e2873d1371972
출처 데이터셋
uspto-grants-1987_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04657915

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