Ethyl formate → 5-Fluoro-6-oxo-2-(quinolin-6-ylamino)-1,6-dihydropyridin-3-carbonitrile

HRID 340439ノート

反応式

HRID 340439 の反応式
[CH:1](OCC)=O.[H-].[Na+].C([O:11][CH2:12][CH2:13][F:14])(=O)C.[C:15]([CH2:17][C:18]([NH:20][C:21]1[CH:22]=[C:23]2[C:28](=[CH:29][CH:30]=1)[N:27]=[CH:26][CH:25]=[CH:24]2)=[NH:19])#[N:16]>C(O)C.CCCCCC>[F:14][C:13]1[C:12](=[O:11])[NH:19][C:18]([NH:20][C:21]2[CH:22]=[C:23]3[C:28](=[CH:29][CH:30]=2)[N:27]=[CH:26][CH:25]=[CH:24]3)=[C:17]([C:15]#[N:16])[CH:1]=1

参加物

7

反応物 4

HCID 8025Ethyl formateHCID 10016Ethanol, 2-fluoro-, 1-acetateHCID 24758Sodium hydrideHCID 178511140HCID 178511140、化合物

生成物 1

HCID 686063515-Fluoro-6-oxo-2-(quinolin-6-ylamino)-1,6-dihydropyridin-3-carbonitrile

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒2 回HCID 8058Hexane溶媒

実験手順

Ethyl formate (16.1 ml) was added to a hexane (40 ml) suspension containing sodium hydride (60% in oil, 2.4 g) at room temperature, and then fluoroethyl acetate (3.86 ml) was added dropwise under ice cooling, followed by stirring at room temperature for 15 minutes. Ethanol (50 ml) was added to the reaction mixture, and then an ethanol (50 ml) solution containing 2-cyano-N-(quinolin-6-yl)acetamidine (4.20 g) was added dropwise, followed by stirring at 80° C. for 2 hours. The reaction mixture was cooled to room temperature. Then, solid matter was collected by filtration and washed with ethyl acetate, and a yellow solid of 5-fluoro-6-oxo-2-(quinolin-6-ylamino)-1,6-dihydropyridin-3-carbonitrile (3.71 g) was thus obtained.

後処理

  1. additionwas added dropwise
  2. stirringby stirring at 80° C. for 2 hours
  3. temperatureThe reaction mixture was cooled to room temperature
  4. filtrationThen, solid matter was collected by filtration
  5. washwashed with ethyl acetate

出典と根拠

ORDレコード
ord-0af78f720882434f8794c4e806fad912
出典データセット
uspto-grants-2014_11
特許番号
US08895585B2

反応ノート

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