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Ethyl 4-chloroacetoacetate → Ethyl 2-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)acetate

HRID 2206332
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HRID 2206332 반응식
Cl[CH2:2][C:3](=O)[CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6].[CH3:11][C:12]1[C:13]([NH2:19])=[N:14][CH:15]=[C:16]([CH3:18])[N:17]=1>C(O)C>[CH3:18][C:16]1[N:17]=[C:12]([CH3:11])[C:13]2[N:14]([CH:2]=[C:3]([CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6])[N:19]=2)[CH:15]=1
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참가 물질

4

반응물 2

HCID 69484Ethyl 4-chloroacetoacetateHCID 27747642-Amino-3,5-dimethylpyrazine

생성물 1

HCID 89657132Ethyl 2-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)acetate수율 87.8%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
100 °C

실험 절차

A 75 mL pressure vessel was charged with ethyl 4-chloro-3-oxo-butyrate (4 g, 24.4 mmol), 3,5-dimethylpyrazin-2-amine (3 g, 24.4 mmol) and 200 proof ethanol (24 mL). After stirring at 100° C. in an oil bath for 16 hours, the reaction mixture was concentrated, diluted with dichloromethane and a saturated sodium bicarbonate solution. The organic layer was separated and the aqueous layer was extracted with dichloromethane twice. The combined organic layers were dried over anhydrous sodium sulfate, filtered, concentrated, and purified on silica gel. Elution with a gradient mixture of dichloromethane and methanol yielded ethyl 2-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)acetate as a light brown solid (5 g). MS m/z 234 [M+H]+.

후처리

  1. concentrationthe reaction mixture was concentrated
  2. additiondiluted with dichloromethane
  3. customThe organic layer was separated
  4. extractionthe aqueous layer was extracted with dichloromethane twice
  5. dry with materialThe combined organic layers were dried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. custompurified on silica gel
  9. washElution
  10. additionwith a gradient mixture of dichloromethane and methanol

출처 및 근거

ORD 기록
ord-e52cce5288d7459ab66ec5f1a1a4f47a
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09371336B2

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