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Ethyl isothiocyanatoformate → HCID 58534942, 화합물

HRID 2197420
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HRID 2197420 반응식
[CH3:1][O:2][C:3]1[N:8]=[C:7]([NH2:9])[C:6]([O:10][CH3:11])=[CH:5][N:4]=1.[CH3:12][CH2:13][O:14][C:15]([N:17]=[C:18]=[S:19])=[O:16]>C(OCC)(=O)C>[CH3:1][O:2][C:3]1[N:8]=[C:7]([NH:9][C:18]([NH:17][C:15](=[O:16])[O:14][CH2:13][CH3:12])=[S:19])[C:6]([O:10][CH3:11])=[CH:5][N:4]=1
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참가 물질

4

반응물 2

HCID 85320Ethyl isothiocyanatoformate2회HCID 2503704-Pyrimidinamine, 2,5-dimethoxy-

생성물 1

HCID 58534942HCID 58534942, 화합물수율 89%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

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온도
78 °C

실험 절차

2,5-Dimethoxypyrimidin-4-amine (6) (3 g, 0.0193 moles) was dissolved in 18 g of ethyl acetate. Ethyl isothiocyanatidocarbonate (2.77 g, 0.0208 moles) was added in one portion. The solution was heated to 78° C. and held at that temperature for 11 h. An additional 1.4 g of the ethyl isothiocyanatidocarbonate was added and the mixture heated for 2.5 h. The mixture was allowed to cool to 22° C. and filtered. The resulting solid was washed with ethyl acetate (20 mL) and dried to a constant weight in a fume hood to afford the title compound as a yellow solid (4.81 g, 89%): 13C NMR (DMSO-d6, 100 MHz) δ 177.5, 158.4, 153.3, 149.5, 142.3, 139.5, 62.6, 57.6, 55.2, 14.4; HRMS (ESI), calcd for C10H14N4O4S, 286.0736; found, 286.0727.

후처리

  1. temperaturethe mixture heated for 2.5 h
  2. temperatureto cool to 22° C.
  3. filtrationfiltered
  4. washThe resulting solid was washed with ethyl acetate (20 mL)
  5. customdried to a constant weight in a fume hood

출처 및 근거

ORD 기록
ord-9e2eeaaf4e4642ab94f797c2aea690a2
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08338596B2

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