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Carbon Disulfide → [1,3]Thiazolo[5,4-b]pyridine-2(1H)-thione

HRID 344711
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HRID 344711 반응식
[NH2:1][C:2]1[C:3](Cl)=[N:4][CH:5]=[CH:6][CH:7]=1.[C:9](=[S:11])=[S:10]>CN(C=O)C>[NH:1]1[C:2]2[CH:7]=[CH:6][CH:5]=[N:4][C:3]=2[S:11][C:9]1=[S:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6348Carbon DisulfideHCID 805282-Chloro-3-pyridylamine

생성물 1

HCID 2782239[1,3]Thiazolo[5,4-b]pyridine-2(1H)-thione수율 90%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of 6.43 g (50.0 mmols) of 3-amino-2-chloropyridine, 50 ml of carbon disulfide and 50 ml of DMF was heated under reflux for 6 days. An excess of carbon disulfide was evaporated under reduced pressure, and the residue was poured into 300 ml of ice water with stirring. The precipitated crystals was taken out by filtration and dried to afford 7.57 g (yield: 90%) of pyrido[3,2-d]thiazo-line-2-thione.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 6 days
  3. customAn excess of carbon disulfide was evaporated under reduced pressure
  4. additionthe residue was poured into 300 ml of ice water
  5. filtrationThe precipitated crystals was taken out by filtration
  6. customdried

출처 및 근거

ORD 기록
ord-8942ed11f1d2461db98673c7d5d75d84
출처 데이터셋
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05053408

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