참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Bromotheophylline | HCID 11808 | — |
| 반응물 | 5-Aminopentan-1-ol | HCID 75634 | — |
| 용매 | P-Xylene | HCID 7809 | — |
| 생성물 | 8-(5-Hydroxypentylamino)theophylline | HCID 22413185 | 66.6% |
반응 단계
A solution of 5.16 grams of 8-bromotheophylline and 5.15 grams of 5-amino-1 pentanol in 18 ml of p-xylene was refluxed for 18 hours. The reaction solution was allowed to cool and upon cooling to room temperature formed a solid/liquid mixture. The xylene was decanted and the solid was washed with pentane (3×40 ml). The resulting solid was stirred in 20 ml of water for 30 minutes and filtered to collect the solid material. The collected solid material was washed with water (3×20 ml), and dried to provide 3.73 g of 8-(5-hydroxypentylamino)theophylline. To a solution of 1.12 g of 8-(5-hydroxypentylamino)theophylline in 15 ml of anhydrous N,N-dimethylformamide (DMF) was added 0.516 g of succinic anhydride and 0.2 g of 4-dimethylamino pyridine (DMAP). The mixture was stirred with a magnetic stirrer overnight at room temperature under anhydrous conditions. The colorless solid that precipitated was collected by vacuum filtration, washed with dichloromethane and air dried to provide 1.20 g of theophylline-8-N-(5-hydroxypentylamino)-O-succinic acid ester. This solid was recrystallized from a boiling 1:1 propanol/water mixture and dried over calcium sulfate to provide a colorless solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05512433 |
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| 출처 데이터셋 | uspto-grants-1996_04 |
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| ORD ID | ord-e6f5815df17e435c932248ba542e782f |
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| 출처 메모 | uspto-grants-1996_04 |
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