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Diethylamine → HCID 14372173、化合物

HRID 1383017
ノート
印刷プレビュー

反応式

HRID 1383017 の反応式
[O:1]1[C:5]2=[N:6][CH:7]=[C:8]([C:10]([OH:12])=O)[CH:9]=[C:4]2[CH:3]=[CH:2]1.C(Cl)(=O)C(Cl)=O.[CH2:19]([NH:21][CH2:22][CH3:23])[CH3:20]>C(Cl)Cl.CN(C)C=O>[CH2:19]([N:21]([CH2:22][CH3:23])[C:10]([C:8]1[CH:9]=[C:4]2[CH:3]=[CH:2][O:1][C:5]2=[N:6][CH:7]=1)=[O:12])[CH3:20]
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 8021DiethylamineHCID 65578Oxalyl chlorideHCID 14372168Furo[2,3-b]pyridine-5-carboxylic acid

生成物 1

HCID 14372173HCID 14372173、化合物収率 124.5%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide触媒HCID 6344Dichloromethane溶媒

実験手順

To a suspension of furo[2,3-b]pyridine-5-carboxylic acid (3.30 g, 20.2 mmol) in methylene chloride (80 mL), under a nitrogen atmosphere at room temperature, was added oxalyl chloride (4.2 mL, 48 mmol) and then four drops of dimethylformamide. The reaction mixture was stirred until gas evolution ceased (4-5 hours) and a clear solution resulted. This solution was evaporated in vacuo and the excess oxalyl chloride chased by evaporation with benzene. The residue was dissolved in chloroform (50 mL) and diethylamine (5.2 mL, 50 mmol) was added carefully. After 0.5 hours, the chloroform solution was washed with dilute hydrochloric acid, filtered through a pad of charcoal and evaporated to give crude product (5.49 g). This oil was distilled under vacuum to give purified product (3.62 g, 82% yield), bp: 168°-170° C./1.6 mmHg.

後処理

  1. custom(4-5 hours)
  2. customa clear solution resulted
  3. customThis solution was evaporated in vacuo
  4. customthe excess oxalyl chloride chased by evaporation with benzene
  5. dissolutionThe residue was dissolved in chloroform (50 mL)
  6. washthe chloroform solution was washed with dilute hydrochloric acid
  7. filtrationfiltered through a pad of charcoal
  8. customevaporated

出典と根拠

ORDレコード
ord-fc6eda01c23148029ba41eacf5c7f6bd
出典データセット
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04808595

反応ノート

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