참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzenamine, 2,6-dimethoxy- | HCID 95940 | — |
| 반응물 | Pyrimidine-2,4,5,6(1H,3H)-tetrone tetrahydrate | HCID 12338093 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 5-(4-Amino-3,5-dimethoxyphenyl)-5-hydroxybarbituric acid | HCID 21290280 | 91.7% |
반응 단계
25 g of 2,6-dimethoxyaniline were added to a solution of 35 g of alloxan tetrahydrate in 120 ml of water. While stirring vigorously, the initially heterogeneous mixture changed after one hour into a brown solution from which grey crystals separated after a short time. The reaction mixture was stirred at room temperature for an additional 24 hours until dimethoxyaniline was no longer detectable according to thin-layer chromatography (cyclohexane/ethyl acetate/water=60:30:1). The reaction mixture was suction filtered, the residue on the suction filter was suspended with 4 portions of water to 80 ml and sucked dry. The solid was dried at 100°/16 mbar for 16 hours. There were obtained 44.2 g of 5-(4-amino-3,5-dimethoxyphenyl)-5-hydroxybarbituric acid as a light grey powder of m.p. 240°-243° (under decomposition). For purification, the powder can be recrystallized from 1-butanol, there being obtained a product of m.p. 242°-244° (decomposition).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04775756 |
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| 출처 데이터셋 | uspto-grants-1988_10 |
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| ORD ID | ord-0cd81c599a374e4b8c37613dc6cc0a5d |
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| 출처 메모 | uspto-grants-1988_10 |
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