참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl Sulfoxide | HCID 679 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 3-Methylxanthine | HCID 70639 | — |
| 반응물 | 4-Chloro-2,2-dimethylbutanoate | HCID 21753047 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 3-Methyl-7-(methylpivaloyl)xanthine | HCID 21584233 | 90.2% |
반응 단계
This example illustrates a synthesis of 1-(8,9-Oxidohexyl)-3-methyl-7-methylpivaloylxanthine (inventive compound no. 1410). A mixture of 3-methylxanthine (Aldrich, 1.00 g, 6.0 mmol), sodium hydride (145 mg, 6.0 mmol) and dimethyl sulfoxide (20 mL) was stirred until homogeneous (0.5 hours). Chloromethylpivalate (865 mL, 904 mg, 6.0 mmol) was added and the reaction stirred for 18 hours. The reaction mixture was poured into water (70 mL) and then extracted with 25% ethanol/dichloromethane (4×60 mL). The combined organic extracts were dried over sodium sulfate and evaporated under vacuum to a volume of 40 mL. This solution was cooled in icewater, whereupon a thick white precipitate formed. The solid was filtered off under suction and dried under vacuum to yield 1.43 g (90% yield) 3-methyl-7-(methylpivaloyl)xanthine (inventive compound no. 1404).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05866576 |
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| 출처 데이터셋 | uspto-grants-1999_02 |
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| ORD ID | ord-6d684acec1174f1daab1ed470cec0ee7 |
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| 출처 메모 | uspto-grants-1999_02 |
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