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Ammonia → Resiquimod

HRID 1006631
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HRID 1006631 반응식
Cl[C:2]1[C:11]2[N:12]=[C:13]([CH2:20][O:21][CH2:22][CH3:23])[N:14]([CH2:15][C:16]([CH3:19])([CH3:18])[OH:17])[C:10]=2[C:9]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=2[N:3]=1.[NH3:24]>>[NH2:24][C:2]1[C:11]2[N:12]=[C:13]([CH2:20][O:21][CH2:22][CH3:23])[N:14]([CH2:15][C:16]([CH3:19])([CH3:18])[OH:17])[C:10]=2[C:9]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=2[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 222AmmoniaHCID 22672652HCID 22672652, 화합물

생성물 1

HCID 159603Resiquimod

실험 절차

4-Chloro-α,α-dimethyl-2-ethoxymethyl-1H-imidazo[4,5-c]quinoline-1-ethanol (1.0 g, 3 mmol, Example 100) and 7% methanolic ammonia (30 mL) were placed in a steel pressure vessel at about 150-160° C. for 6 hours. The vessel was cooled to below room temperature and the reaction solution removed and treated with methanolic potassium hydroxide. The solution was then evaporated to a low volume and diluted with water. The resulting precipitate was collected, washed with water and dried to provide 0.7 g of the crude product as a solid. The crude product was recrystallized from a mixture of ethyl acetate and methanol to provide a colorless solid.

후처리

  1. temperatureThe vessel was cooled to below room temperature
  2. customthe reaction solution removed
  3. additiontreated with methanolic potassium hydroxide
  4. customThe solution was then evaporated to a low volume
  • additiondiluted with water
  • customThe resulting precipitate was collected
  • washwashed with water
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-dd0c5ef2c86f4ff9962407e84ddb5e3e
    출처 데이터셋
    uspto-grants-2004_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06790961B2

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