참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Chloro-4-nitrophenol | HCID 10283 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 4-Chloro-2-methylthiopyrimidine | HCID 97113 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-Methylsulfanyl-4-(3-chloro-4-nitrophenoxy)-pyrimidine | HCID 67523947 | 64.1% |
반응 단계
160 mg (6.34 mmol) 95% sodium hydride was given to a solution of 1.00 g (5.76 mmol) 3-chloro-4-nitrophenol in 15 ml DMF. Stirring was continued for 30 min. at room temperature. 925 mg (5.76 mmol) 4-chloro-2-methylsulfanyl-pyrimidine was added and the mixture heated to 80° C. for 16 h. The reaction mixture was evaporated, taken up with water and extracted with ethyl acetate. The organic phase was extracted with water, dried (sodium sulphate) and evaporated. The obtained material was dissolved in ethyl acetate and purified by chromatography over silica (ethyl acetate/n-heptane) to give 1.10 g (64%) 4-(3-chloro-4-nitro-phenoxy)-2-methylsulfanyl-pyrimidine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08080552B2 |
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| 출처 데이터셋 | uspto-grants-2011_12 |
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| ORD ID | ord-33c7b7ddca184643b13bb176aaa90e9f |
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| 출처 메모 | uspto-grants-2011_12 |
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