참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | 2-Chloro-4,5-diamino-6-methylpyrimidine | HCID 275295 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 2-Chloro-6,8-dimethylpurine | HCID 10313396 | 635.5% |
반응 단계
After adding 10.1 ml of ortho-triethyl acetate, 0.23 g of para-toluenesulfonic acid and 73 ml of 2-methylpyrrolidone to 7.6 g of 4,5-diamino-2-chloro-6-methylpyrimidine, the mixture was heated at 100° C. and then heated and stirred while removing out of the system the ethanol produced during the reaction. After disappearance of the 4,5-diamino-2-chloro-6-methylpyrimidine, the reaction solution was further heated and stirred at 180° C. for 2 hours. After cooling to room temperature, chloroform was added thereto for dilution. The mixture solution was washed with water and then washed with saturated brine, after which the organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform:methanol=95.5) to obtain 1.55 g of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06919455B2 |
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| 출처 데이터셋 | uspto-grants-2005_07 |
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| ORD ID | ord-6cfa62c9cb6b4b1088f9bed1d4391718 |
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| 출처 메모 | uspto-grants-2005_07 |
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