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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 21279521, 화합물 → HCID 21279508, 화합물

HRID 2291216
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HRID 2291216 반응식
[CH2:1]([S:8][C:9]1[N:13]=[C:12]([S:14][CH:15]([CH3:19])[C:16](O)=[O:17])[NH:11][N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C(OCC)(=O)C>[CH2:1]([S:8][C:9]1[N:13]=[C:12]2[S:14][CH:15]([CH3:19])[C:16](=[O:17])[N:11]2[N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 21279521HCID 21279521, 화합물

생성물 1

HCID 21279508HCID 21279508, 화합물수율 83%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

The product of stage (a) (57.9 g) was added portionwise to polyphosphoric acid (250 ml) at about 100° C. with stirring. Heating was continued for 30 minutes and the solution was then added to ice-water (1 l) and ethyl acetate (300 ml). The ethyl acetate solution was separated, and the aqueous phase was extracted with ethyl acetate. The organic phases were combined, washed with aqueous bicarbonate and water, dried and run down to give 49.3 g of crude product. Recrystallisation from ethanol gave 45.1 g of desired product, mp 85°-87° C.

후처리

  1. temperatureHeating
  2. customThe ethyl acetate solution was separated
extraction
the aqueous phase was extracted with ethyl acetate
  • washwashed with aqueous bicarbonate and water
  • customdried
  • customto give 49.3 g of crude product
  • customRecrystallisation from ethanol
  • 출처 및 근거

    ORD 기록
    ord-50ee2d48c8e34b528b6de0e485df1e1b
    출처 데이터셋
    uspto-grants-1989_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04795483

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