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2,3-Diaminopyridine → HCID 178448403、化合物

HRID 2054443
ノート
印刷プレビュー

反応式

HRID 2054443 の反応式
[NH2:1][C:2]1[C:7]([NH2:8])=[CH:6][CH:5]=[CH:4][N:3]=1.[Cl:9][CH:10]([CH2:14][CH3:15])[C:11](O)=O>O>[Cl:9][CH:10]([C:11]1[NH:1][C:2]2=[N:3][CH:4]=[CH:5][CH:6]=[C:7]2[N:8]=1)[CH2:14][CH3:15]
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

4

反応物 2

HCID 99562,3-DiaminopyridineHCID 201372-Chlorobutyric acid

生成物 1

HCID 178448403HCID 178448403、化合物

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
80 °C

実験手順

5.0 g of 2,3-diaminopyridine in 200 g of polyphosphoric acid are heated at 120° C. for 0.5 h. The solution is cooled to 80° C. and 5.7 ml of 2-chlorobutyric acid are added. Thereafter, the reaction mixture is heated to 130° C. for 22 h. After cooling, the polyphosphoric acid is hydrolysed with water, the mixture is filtered using charcoal and celite and the pH value of the filtrate is adjusted to pH 4 using 9 M aqueous sodium hydroxide solution. The mixture is extracted three times each with 200 ml of ethyl acetate, the combined organic phases are dried using sodium sulfate, concentrated and the residue is purified by chromatography on silica gel (eluent: toluene/ethyl acetate 1:1) to give 5.19 g of the title compound as a colorless, amorpheous solid. M.p. 137° C. TLC: Rf=0.50 (dichloromethane/methanol 10:1).

後処理

  1. temperatureThereafter, the reaction mixture is heated to 130° C. for 22 h
  2. temperatureAfter cooling
  3. filtrationthe mixture is filtered
  4. extractionThe mixture is extracted three times each with 200 ml of ethyl acetate
  5. customthe combined organic phases are dried
  6. concentrationconcentrated
  7. customthe residue is purified by chromatography on silica gel (eluent: toluene/ethyl acetate 1:1)

出典と根拠

ORDレコード
ord-accb37b4f26e4bf2999888ef5285ad22
出典データセット
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07329677B2

反応ノート

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