홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

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

HRID 620743
노트
인쇄 미리보기

반응식

HRID 620743 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-93a513aadfc7470aa6ea4a48e7359a9e
출처 데이터셋
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04822794

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트