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Methane → HCID 178448403、化合物

HRID 2250388
ノート
印刷プレビュー

反応式

HRID 2250388 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.C>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

5

反応物 3

HCID 297MethaneHCID 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 136 ml of water. After reheating to 90° C., charcoal is added under vigorous stirring. Subsequently, the suspension is filtered through a celite pad while still hot (70° C.). The filter cake is rinsed with 100 ml of water and the 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 purified by chromatography on silica gel (eluent: toluene/ethyl acetate 1:1) to give 5.19 g of the title compound as a colorless, amorphous solid. M.p. 137° C. MS: 196.0/198.0 (MH+, 100%/32%). 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. customAfter reheating to 90° C.
  4. filtrationSubsequently, the suspension is filtered through a celite pad while still hot (70° C.)
  5. washThe filter cake is rinsed with 100 ml of water
  6. extractionThe mixture is extracted three times each with 200 ml of ethyl acetate
  7. customthe combined organic phases are dried
  8. concentrationconcentrated
  9. custompurified by chromatography on silica gel (eluent: toluene/ethyl acetate 1:1)

出典と根拠

ORDレコード
ord-18bc8f655b7a45e29587cb2b09ae389a
出典データセット
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07317021B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート