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Tetrahydrofuran → 2-Aminopyridine-4-carbothioamide

HRID 2282157
ノート
印刷プレビュー

反応式

HRID 2282157 の反応式
[NH2:1][C:2]1[CH:7]=[C:6]([C:8]#[N:9])[CH:5]=[CH:4][N:3]=1.P(OCC)(OCC)([S-])=[S:11].O1CCCC1.C(=O)(O)[O-].[Na+]>O>[NH2:1][C:2]1[CH:7]=[C:6]([C:8](=[S:11])[NH2:9])[CH:5]=[CH:4][N:3]=1
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

6

反応物 4

HCID 8028TetrahydrofuranHCID 516892Sodium BicarbonateHCID 1385274Diethyl dithiophosphate, potassium salt2 回HCID 70155242-Aminoisonicotinonitrile

生成物 1

HCID 246938362-Aminopyridine-4-carbothioamide収率 81%

試薬・触媒・溶媒 1

HCID 962Water
溶媒

反応条件

温度
60 °C

実験手順

A mixture of 2-aminopyridine-4-carbonitrile (6.0 g, 50 mmol), O,O′-diethyl dithiophosphate (11 mL, 60 mmol), tetrahydrofuran (25 mL) and water (25 mL) was stirred at 60° C. for 4 hr. To the reaction mixture was added O,O′-diethyl dithiophosphate (2.8 mL, 15 mmol) and the mixture was stirred at 60° C. for 1 day. To the reaction mixture was added aqueous sodium bicarbonate solution, and the mixture was extracted with ethyl acetate. The combined organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the insoluble material was filtered off. The filtrate was concentrated under reduced pressure, and the obtained residue was washed with diisopropyl ether to give the title compound (6.2 g, 81%) as a yellow solid.

後処理

  1. stirringthe mixture was stirred at 60° C. for 1 day
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe combined organic layer was washed with saturated brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. filtrationthe insoluble material was filtered off
  6. concentrationThe filtrate was concentrated under reduced pressure
  7. washthe obtained residue was washed with diisopropyl ether

出典と根拠

ORDレコード
ord-b6ca5242bd964e52875f2137b1e320ce
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09139589B2

反応ノート

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