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Diethylamine → HCID 14372173, 화합물

HRID 1383017
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HRID 1383017 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 8021DiethylamineHCID 65578Oxalyl chlorideHCID 14372168Furo[2,3-b]pyridine-5-carboxylic acid

생성물 1

HCID 14372173HCID 14372173, 화합물수율 124.5%

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 6344Dichloromethane용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-fc6eda01c23148029ba41eacf5c7f6bd
출처 데이터셋
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04808595

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