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2,4-Dichloro-5-(2-((trichloromethyl)thio)phenyl)pyrimidine → 2-Chlorobenzo[4,5]thieno[2,3-d]pyrimidine

HRID 711396
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HRID 711396 반응식
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[S:15]C(Cl)(Cl)Cl)=[CH:4][N:3]=1>CN(C=O)C.O.[Cu]I>[Cl:1][C:2]1[N:7]=[CH:6][C:5]2[C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[S:15][C:4]=2[N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 1183402992,4-Dichloro-5-(2-((trichloromethyl)thio)phenyl)pyrimidine

생성물 1

HCID 918846182-Chlorobenzo[4,5]thieno[2,3-d]pyrimidine수율 38.4%

시약·촉매·용매 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매HCID 962Water용매HCID 6228Dimethylformamide용매

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온도
110 °C

실험 절차

A solution of 2,4-dichloro-5-(2-((trichloromethyl)thio)phenyl)pyrimidine (0.618 g, 1.650 mmol) and copper(I) iodide (0.031 g, 0.165 mmol) in DMF (24.63 ml) was degassed with nitrogen and heated at 110° C. overnight. The reaction solution was cooled to room temperature, diluted with water and filtered. The resulting brown solids were washed with water and a small volume of EtOH. The aqueous layer was extracted twice with EtOAc, combined with the solids, and concentrated in vacuo. The crude product was purified by column chromatography on silica gel, eluted with 10-20% EtOAc/heptanes (v/v), affording 0.14 g (38% yield) of the 2-chlorobenzo[4,5]thieno[2,3-d]pyrimidine as white solids.

후처리

  1. temperatureThe reaction solution was cooled to room temperature
  2. filtrationfiltered
  3. washThe resulting brown solids were washed with water
  4. extractionThe aqueous layer was extracted twice with EtOAc
  5. concentrationconcentrated in vacuo
  6. customThe crude product was purified by column chromatography on silica gel
  7. washeluted with 10-20% EtOAc/heptanes (v/v)

출처 및 근거

ORD 기록
ord-fca663239ad443d5b3f0140c3f657992
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181270B2

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