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2,2-Dimethyl-1,3-dioxane-4,6-dione → 3-(2,2-Dimethyl-4,6-dioxo-1,3-dioxan-5-ylidene)amino-4-carbethoxy-pyrazole

HRID 1026901
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HRID 1026901 반응식
[CH3:1][C:2]1([CH3:10])[O:9][C:7](=[O:8])[CH2:6][C:4](=[O:5])[O:3]1.[CH:11](OCC)(OCC)OCC.[NH2:21][C:22]1[C:26]([C:27]([O:29][CH2:30][CH3:31])=[O:28])=[CH:25][NH:24][N:23]=1>C1(C)C=CC=CC=1>[CH3:1][C:2]1([CH3:10])[O:9][C:7](=[O:8])[C:6](=[CH:11][NH:21][C:22]2[NH:23][N:24]=[CH:25][C:26]=2[C:27]([O:29][CH2:30][CH3:31])=[O:28])[C:4](=[O:5])[O:3]1
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참가 물질

5

반응물 3

HCID 162492,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 31214Ethyl orthoformateHCID 178469928HCID 178469928, 화합물

생성물 1

HCID 5407593-(2,2-Dimethyl-4,6-dioxo-1,3-dioxan-5-ylidene)amino-4-carbethoxy-pyrazole수율 88%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

Meldrum's acid (15.3 g, 106 mmol) was dissolved in toluene (450 mL), triethyl orthoformate (17.6 mL, 106 mmol) was added, and the mixture was heated under reflux for 2 hr. The reaction mixture was allowed to cool to room temperature, ethyl 3-amino-4-pyrazolecarboxylate (15 g, 96.7 mmol) was added, and the mixture was heated under reflux for 3 hr. The reaction mixture was allowed to cool to room temperature, and stirred at room temperature for 10 hr. The precipitated crystals were collected by filtration, washed with diisopropylether (100 mL), and dried under reduced pressure at 40° C. overnight to give the title compound (26.3 g, 88%).

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 2 hr
  3. temperaturethe mixture was heated
  4. temperatureunder reflux for 3 hr
  5. temperatureto cool to room temperature
  6. filtrationThe precipitated crystals were collected by filtration
  7. washwashed with diisopropylether (100 mL)
  8. customdried under reduced pressure at 40° C. overnight

출처 및 근거

ORD 기록
ord-1320916e2995492a9e0c9bc515a40fab
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08729264B2

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