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3-Pyridinecarboximidic acid, N-cyano-, 1-methylethyl ester → N-cyano-N'-(4-ethyl-2,4-hexadien-1-yl)-3-pyridinecarboximidamide

HRID 2396900
ノート
印刷プレビュー

反応式

HRID 2396900 の反応式
[CH2:1]([C:3](=[CH:8][CH3:9])[CH:4]=[CH:5][CH2:6][NH2:7])[CH3:2].[C:10]([N:12]=[C:13]([C:18]1[CH:19]=[N:20][CH:21]=[CH:22][CH:23]=1)OC(C)C)#[N:11].C[O-].[Na+]>CO.O>[C:10]([NH:12][C:13]([C:18]1[CH:19]=[N:20][CH:21]=[CH:22][CH:23]=1)=[N:7][CH2:6][CH:5]=[CH:4][C:3]([CH2:1][CH3:2])=[CH:8][CH3:9])#[N:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 100812013-Pyridinecarboximidic acid, N-cyano-, 1-methylethyl esterHCID 10942334Sodium MethoxideHCID 539452134-Ethyl-2,4-hexadien-1-ylamine

生成物 1

HCID 54082574N-cyano-N'-(4-ethyl-2,4-hexadien-1-yl)-3-pyridinecarboximidamide収率 80.8%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒2 回
HCID 962
Water
溶媒

実験手順

To a solution of crude 4-ethyl-2,4-hexadien-1-ylamine (1.38 g) and isopropyl N-cyano-3-pyridinecarboximidate (1.74 g) in methanol (35 ml) at room temperature was added 28% sodium methoxide in methanol (2.13 g). After 10 minutes, the mixture was diluted with water and extracted three times with dichloromethane. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and evaporated in vacuo. The residue was chromatographed on silica gel (5% methanol in dichloromethane) to give N-cyano-N'-(4-ethyl-2,4-hexadien-1-yl)-3-pyridinecarboximidamide (1.89 g) as an oil.

後処理

  1. extractionextracted three times with dichloromethane
  2. washThe organic layer was washed with brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. customevaporated in vacuo
  5. customThe residue was chromatographed on silica gel (5% methanol in dichloromethane)

出典と根拠

ORDレコード
ord-e793817070e84fc5b3bbbe3d1d9d06b3
出典データセット
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05495023

反応ノート

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