참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Morpholine | HCID 8083 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 1-Iodooctane | HCID 12380 | — |
| 반응물 | 8-Chloroxanthine | HCID 26103 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 8-Chloro-3-octyl-3,7-dihydro-1H-purine-2,6-dione | HCID 59299546 | — |
반응 단계
8-Chloro-3,7-dihydro-1H-purine-2,6-dione (100 mg, 0.44 mmol) was stirred with sodium carbonate (52 mg, 0.49 mmol) in dry DMF (3 ml) for 20 min., then 1-iodooctane (118 mg, 0.49 mmol) was added and the mixture was stirred under nitrogen at 40 C for 65 h. After cooling to room temperature, the mixture was thoroughly degassed by evacuating the vessel and refilling with nitrogen several times. Tetrakis(triphenylphosphine)palladium(0) (102 mg, 0.09 mmol) was added, the mixture degassed again and then morpholine (0.385 ml, 4.4 mmol) added and stirring continued for 6.5 h. 2M HCl and EtOAc were added, and the 2-phase system was filtered. The product was present predominantly in the filtered solid, which was recrystallised from THF-acetonitrile, followed by MeOH, with filtration, to afford the pure title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08268839B2 |
|---|
| 출처 데이터셋 | uspto-grants-2012_09 |
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| ORD ID | ord-485829e54dfc466bafcf0e4400abf024 |
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| 출처 메모 | uspto-grants-2012_09 |
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