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Ethanol → HCID 20093979, 화합물

HRID 273783
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인쇄 미리보기

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HRID 273783 반응식
[Cl:1][CH2:2][C:3]1[N:4]=[C:5]([NH:12][NH2:13])[C:6]2[S:11][CH:10]=[CH:9][C:7]=2[N:8]=1.[CH2:14](O)C>C([O-])([O-])OCC>[Cl:1][CH2:2][C:3]1[N:4]2[CH:14]=[N:13][N:12]=[C:5]2[C:6]2[S:11][CH:10]=[CH:9][C:7]=2[N:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 702EthanolHCID 20094178HCID 20094178, 화합물

생성물 1

HCID 20093979HCID 20093979, 화합물

시약·촉매·용매 1

HCID 53630039Ethylorthoformate용매

반응 조건

온도
125 °C

실험 절차

4. 15.7 g of 2-(chloromethyl)-4-hydrazinothieno[3,2-d]pyrimidine are suspended in 280ml of ethyl orthoformate. The suspension is heated (bath temp. 125° C.) while stirring and the ethanol which results is distilled off. After 3 h., the mixture is cooled to 0° C., the precipitate is filtered off and washed with ethanol. The product is dried in a vacuum. There are obtained 15.2 g of 5-(chloromethyl)thieno[2,3-e][1,2,4]triazolo[4,3-c]-pyrimidine. m.p. above 400° C. (dec.).

후처리

  1. distillationis distilled off
  2. temperaturethe mixture is cooled to 0° C.
  3. filtrationthe precipitate is filtered off
  4. washwashed with ethanol
  5. customThe product is dried in a vacuum

출처 및 근거

ORD 기록
ord-9fad027ca04f4e48a3bdb6c8122eedd6
출처 데이터셋
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05387585

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