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Sodium Methoxide → HCID 18507453, 화합물

HRID 1356133
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HRID 1356133 반응식
[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[O:9][C:10](Br)=[CH:11][CH:12]=2)[C:5]([C:14]#[N:15])=[C:4]([S:16][CH3:17])[N:3]=1.[CH3:18][O-:19].[Na+]>COCCOC>[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[O:9][C:10]([O:19][CH3:18])=[CH:11][CH:12]=2)[C:5]([C:14]#[N:15])=[C:4]([S:16][CH3:17])[N:3]=1
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참가 물질

4

반응물 2

HCID 10942334Sodium MethoxideHCID 18507285HCID 18507285, 화합물

생성물 1

HCID 18507453HCID 18507453, 화합물수율 87.6%

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

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온도
50 °C

실험 절차

To a stirred solution of 493 mg (1.58 mmol) 2-amino-4-(5-bromo-furan-2-yl)-6-methylsulfanyl-pyrimidine-5-carbonitrile in 10 ml DME was added 2.1 ml (11,3 mmol) sodium methylate solution (5.4M in methanol) and the mixture heated at 50° C. for 1 h. The reaction mixture was then poured into 100 ml ice-water and the resulting precipitate collected by filtration and washed with water. Chromatography (ethyl acetate/hexane 1/1) afforded 363 mg (87%) 2-amino-4-(5-methoxy-furan-2-yl)-6-methylsulfanyl-pyrimidine-5-carbonitrile as a light yellow crystalline solid. EI-MS m/e (%): 262 (M+, 100).

후처리

  1. filtrationthe resulting precipitate collected by filtration
  2. washwashed with water

출처 및 근거

ORD 기록
ord-715e1473314b4512b7ce9584784ea5b8
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06586441B2

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