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Acetamidine monohydrochloride → Ethyl 2,4-dimethylpyrimidine-5-carboxylate

HRID 1408520
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인쇄 미리보기

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HRID 1408520 반응식
CN([CH:4]=[C:5]([C:11](=O)[CH3:12])[C:6]([O:8][CH2:9][CH3:10])=[O:7])C.Cl.[C:15]([NH2:18])(=[NH:17])[CH3:16].CC[O-].[Na+]>CCO>[CH3:16][C:15]1[N:18]=[C:11]([CH3:12])[C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][N:17]=1
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참가 물질

5

반응물 3

HCID 67170Acetamidine monohydrochlorideHCID 2723922Sodium ethoxideHCID 3806790Ethyl 2-acetyl-3-(dimethylamino)acrylate

생성물 1

HCID 295888Ethyl 2,4-dimethylpyrimidine-5-carboxylate수율 42.6%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Intermediate 51 (17.6 g, 95 mmol) and acetamidine hydrochloride (17.6 g, 95 mmol), were dissolved in EtOH and added NaOEt (6.5 g, 95 mmol). This mixture was refluxed for 4 h. After that, ethanol removed on rotavapour followed by work-up (AcOEt/H2O) to obtain the crude. Crude was purified by column chromatography using 60-120 mesh silicagel and AcOEt and Petether (25:75) as eluent to obtain the title compound (7.3 g).

후처리

  1. temperatureThis mixture was refluxed for 4 h
  2. customAfter that, ethanol removed on rotavapour
  3. customto obtain the crude
  4. customCrude was purified by column chromatography

출처 및 근거

ORD 기록
ord-a434670dd69b4fbba7546237ab92a269
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08921364B2

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