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Sodium Methoxide → 2-Methoxy-4-sec. butylamino-5nitro-6-methylpyrimidine

HRID 597466
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HRID 597466 반응식
Cl[C:2]1[N:7]=[C:6]([NH:8][CH:9]([CH2:11][CH3:12])[CH3:10])[C:5]([N+:13]([O-:15])=[O:14])=[C:4]([CH3:16])[N:3]=1.[CH3:17][O-:18].[Na+]>CO>[CH3:17][O:18][C:2]1[N:7]=[C:6]([NH:8][CH:9]([CH2:11][CH3:12])[CH3:10])[C:5]([N+:13]([O-:15])=[O:14])=[C:4]([CH3:16])[N:3]=1
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참가 물질

4

반응물 2

HCID 10942334Sodium MethoxideHCID 188014492-Chloro-4-sec. butylamino-5-nitro-6-methylpyrimidine

생성물 1

HCID 214450672-Methoxy-4-sec. butylamino-5nitro-6-methylpyrimidine수율 73.1%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

17.1 g of 2-chloro-4-sec. butylamino-5-nitro-6-methyl-pyrimidine (0.07 mole) are dissolved in 200 ml of methanol. To this solution is added a solution of 8.1 g of sodium methylate (0.15 mole) in 100 ml of methanol and the mixture is boiled overnight at 100° C bath temperature. After it has been cooled, the solution is evaporated and the resultant red substance is treated with ether and then filtered over Hyflo. The filter residue is washed 5 times with ether and the combined ethereal extracts are then evaporated to yield 12.3 g of 2-methoxy-4-sec. butylamino-5nitro-6-methylpyrimidine which boils at 110° C at 0.001 Torr (=73% yield).

후처리

  1. temperatureAfter it has been cooled
  2. customthe solution is evaporated
  3. additionthe resultant red substance is treated with ether
  4. filtrationfiltered over Hyflo
  5. washThe filter residue is washed 5 times with ether
  6. customthe combined ethereal extracts are then evaporated

출처 및 근거

ORD 기록
ord-dccb631b73f543d3b8d59a1c7c4dbf68
출처 데이터셋
uspto-grants-1977_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04014677

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