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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethyl bromopyruvate → HCID 68780924, 화합물

HRID 1878460
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HRID 1878460 반응식
[I:1][C:2]1[CH:3]=[CH:4][C:5]([NH2:9])=[N:6][C:7]=1[CH3:8].Br[CH2:11][C:12](=O)[C:13]([O:15][CH2:16][CH3:17])=[O:14]>C(COC)OC>[I:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([C:11]([C:5]3[CH:4]=[CH:3][CH:2]=[CH:7][N:6]=3)=[C:12]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[N:9]=2)[C:7]=1[CH3:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 66144Ethyl bromopyruvateHCID 9596135-Iodo-6-methylpyridin-2-amine

생성물 1

HCID 68780924HCID 68780924, 화합물

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

반응 조건

온도
20 °C

실험 절차

To a suspension of 2 g of 5-iodo-6-methylpyridine-2-amine in 15 mL of dimethoxyethane are added 1.3 mL of ethyl bromopyruvate. The reaction mixture is stirred at 20° C. for 16 hours and then concentrated to dryness, taken up in 15 mL of ethanol, refluxed for 2.5 hours and finally concentrated under reduced pressure. The residue is taken up in a mixture of dichloromethane and saturated sodium bicarbonate solution. The organic phase is dried over magnesium sulfate and concentrated to dryness under reduced pressure to give 2.77 g of ethyl 6-iodo-5-methyl(pyrid-2-yl)imidazo[1,2-a]pyridine-2-carboxylate in the form of a beige-coloured solid.

후처리

  1. concentrationconcentrated to dryness
  2. temperaturerefluxed for 2.5 hours
  3. concentrationfinally concentrated under reduced pressure
  4. additionThe residue is taken up in a mixture of dichloromethane and saturated sodium bicarbonate solution
  5. dry with materialThe organic phase is dried over magnesium sulfate
  6. concentrationconcentrated to dryness under reduced pressure

출처 및 근거

ORD 기록
ord-514273dccb134c478054a75931c48c86
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08314109B2

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