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Dimethyl Sulfate → 7-Bromo-4-methyl-4H-pyrido[3,2-b][1,4]oxazin-3-one

HRID 1607558
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HRID 1607558 반응식
[Br:1][C:2]1[CH:11]=[N:10][C:9]2[NH:8][C:7](=[O:12])[CH2:6][O:5][C:4]=2[CH:3]=1.[Li]N([Si](C)(C)C)[Si](C)(C)[CH3:16].COS(OC)(=O)=O>C1COCC1>[CH3:16][N:8]1[C:7](=[O:12])[CH2:6][O:5][C:4]2[CH:3]=[C:2]([Br:1])[CH:11]=[N:10][C:9]1=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6497Dimethyl SulfateHCID 159259837-bromo-2H,3H,4H-pyrido(3,2-b)(1,4)oxazin-3-oneHCID 178418261HCID 178418261, 화합물

생성물 1

HCID 159259847-Bromo-4-methyl-4H-pyrido[3,2-b][1,4]oxazin-3-one

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a suspension of 5 g of 7-bromo-2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one (0.022 mole) in 90 ml of THF is added 24 ml of LiN(TMS)2 (0.024 mole) in THF. The homogenous solution is maintained under nitrogen at room temperature for 20 min., 3.03 g (0.024 mole) of dimethylsulfate is added and the reaction mixture allowed to stir overnight. The reaction mixture is then quenched with 20 ml of sat. ammonium chloride and extracted with 3×80 ml ethyl acetate. The ethyl acetate is then washed with 3×30 ml sat. ammonium chloride, dried over sodium sulfate and concentrated to obtain off white product which is used directly in the next step.

후처리

  1. customThe reaction mixture is then quenched with 20 ml of sat. ammonium chloride
  2. extractionextracted with 3×80 ml ethyl acetate
  3. washThe ethyl acetate is then washed with 3×30 ml sat. ammonium chloride
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated
  6. customto obtain off white product which

출처 및 근거

ORD 기록
ord-e13623d82d2b4295b8ce480600352ced
출처 데이터셋
uspto-grants-1989_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04866074

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