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(Ethylsulfonyl)ethene → 2-(2'-Ethylsulfonylethyl)-4-cyano-5,6-diphenyl-3-(2H)-pyridazinone

HRID 463970
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HRID 463970 반응식
[C:1]([C:3]1[C:4](=[O:21])[NH:5][N:6]=[C:7]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:8]=1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)#[N:2].[CH2:22]([S:24]([CH:27]=[CH2:28])(=[O:26])=[O:25])[CH3:23]>N1C=CC=CC=1>[CH2:22]([S:24]([CH2:27][CH2:28][N:5]1[C:4](=[O:21])[C:3]([C:1]#[N:2])=[C:8]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[C:7]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[N:6]1)(=[O:26])=[O:25])[CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 74680(Ethylsulfonyl)etheneHCID 957574-Pyridazinecarbonitrile, 2,3-dihydro-3-oxo-5,6-diphenyl-

생성물 1

HCID 135335082-(2'-Ethylsulfonylethyl)-4-cyano-5,6-diphenyl-3-(2H)-pyridazinone수율 72.7%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

8.0 grams (0.0175 mole) of the product of Example 1 was reacted with 2.1 grams of ethyl-vinyl sulfone in 60 mls of pyridine. This solution was heated on a steam bath for 2 hours, cooled and the solvent distilled at reduced pressure. The residual oil was taken up in ethyl alcohol. 5.0 grams (72% yield) of a solid precipitated and was filtered, washed with petroleum ether and air dried. The infrared spectrum showed the nitrile band at 4.5μ, the carbonyl band at 6.0μ, the SO2 band at 8.7μ.

후처리

  1. temperatureThis solution was heated on a steam bath for 2 hours
  2. temperaturecooled
  3. distillationthe solvent distilled at reduced pressure

출처 및 근거

ORD 기록
ord-b64e44dccc5545a2ae730aec6463de69
출처 데이터셋
uspto-grants-1985_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04545810

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