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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1721551생성일: 2026년 10월 26일

Bromotheophylline → 8-(5-Hydroxypentylamino)theophylline

https://huagongshe.com/reaction/1721551

반응식

참여 물질

역할이름HCID투입량
반응물BromotheophyllineHCID 11808—
반응물5-Aminopentan-1-olHCID 75634—
용매P-XyleneHCID 7809—
생성물8-(5-Hydroxypentylamino)theophyllineHCID 2241318566.6%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05512433
출처 데이터셋uspto-grants-1996_04
ORD IDord-e6f5815df17e435c932248ba542e782f
출처 메모uspto-grants-1996_04