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Methanol → Methyl 4-(3-oxo-2,3-dihydro-1,2,4-triazin-6-yl)benzoate

HRID 500216
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HRID 500216 반응식
C(O[CH:4](OCC)[C:5]([C:7]1[CH:16]=[CH:15][C:10]([C:11]([O:13][CH3:14])=[O:12])=[CH:9][CH:8]=1)=O)C.Cl.[NH2:21][NH:22][C:23]([NH2:25])=[O:24].C(N(CC)C(C)C)(C)C.CO>ClCCCl.C(Cl)Cl>[O:24]=[C:23]1[N:25]=[CH:4][C:5]([C:7]2[CH:8]=[CH:9][C:10]([C:11]([O:13][CH3:14])=[O:12])=[CH:15][CH:16]=2)=[N:21][NH:22]1
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참가 물질

7

반응물 4

HCID 887MethanolHCID 11236Semicarbazide hydrochloride2회HCID 81531DiisopropylethylamineHCID 59216300Methyl 4-(diethoxyacetyl)benzoate

생성물 1

HCID 59216301Methyl 4-(3-oxo-2,3-dihydro-1,2,4-triazin-6-yl)benzoate

시약·촉매·용매 2

HCID 111,2-Dichloroethane
용매
HCID 6344Dichloromethane용매

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온도
95 °C

실험 절차

A mixture of methyl 4-(diethoxyacetyl)benzoate (15.4 g, 0.0578 mol), semicarbazide hydrochloride (7.1 g, 0.064 mol), N,N-diisopropylethylamine (12 mL, 0.069 mol) in 1,2-dichloroethane (150 mL), and methanol (2 mL) was heated at 95° C. for 4 h. To the mixture was added an additional 0.1 equivalents of semicarbazide hydrochloride. The mixture was stirred at 95° C. for 1 h. After cooling to RT, the mixture was diluted with methylene chloride and washed with water, brine, dried over Na2SO4, filtered, and concentrated. The residue was refluxed with acetic acid (100 mL) and water (1.0 mL) overnight. The mixture was concentrated to yield quantitative crude material which was directly used in the next step.

후처리

  1. temperatureAfter cooling to RT
  2. washwashed with water, brine
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. temperatureThe residue was refluxed with acetic acid (100 mL) and water (1.0 mL) overnight
  7. concentrationThe mixture was concentrated
  8. customto yield quantitative crude material which

출처 및 근거

ORD 기록
ord-5abd7da1945947bf91330e2f575953e7
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07767675B2

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