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Hydrochloric Acid → 10-Trifluoromethyl-1H-pyrimido[5,4,3-kl]phenothiazine-1,3-(2H)-dione

HRID 1658061
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HRID 1658061 반응식
CS[C:3]1[N:18]2[C:19]3[C:10]([S:11][C:12]4[CH:13]=[CH:14][C:15]([C:20]([F:23])([F:22])[F:21])=[CH:16][C:17]=42)=[CH:9][CH:8]=[CH:7][C:6]=3[C:5](=[O:24])[N:4]=1.Cl.C([OH:28])C>>[F:21][C:20]([F:23])([F:22])[C:15]1[CH:14]=[CH:13][C:12]2[S:11][C:10]3[C:19]4=[C:6]([C:5](=[O:24])[NH:4][C:3](=[O:28])[N:18]4[C:17]=2[CH:16]=1)[CH:7]=[CH:8][CH:9]=3
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 702EthanolHCID 12223714HCID 12223714, 화합물

생성물 1

HCID 1222371510-Trifluoromethyl-1H-pyrimido[5,4,3-kl]phenothiazine-1,3-(2H)-dione

실험 절차

A stirred suspension of 53.6 g. (0.146 mol.) of 1-methylmercapto-10-trifluoromethyl-3H-pyrimido[5,4,3-kl]phenothiazine-3-one in 240 ml. of concentrated hydrochloric acid and 800 ml. of ethanol was heated under reflux for four hours. The reaction mixture was concentrated to approximately one-half its original volume by boiling off the excess solvents and chilled. The product was collected by filtration and washed thoroughly with water to give the title compound, m.p. 278°-280° (ethanol).

후처리

  1. addition
A stirred suspension of 53.6 g
  • temperatureunder reflux for four hours
  • concentrationThe reaction mixture was concentrated to approximately one-half its original volume
  • temperaturechilled
  • filtrationThe product was collected by filtration
  • washwashed thoroughly with water
  • 출처 및 근거

    ORD 기록
    ord-00e4f8b5e2a945929064b175707d6ed3
    출처 데이터셋
    uspto-grants-1976_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US03962438

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