참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Dichloromethane | HCID 6344 | — |
| 반응물 | Potassium Acetate | HCID 517044 | — |
| 반응물 | 3-Chloromethyl-5-dichloromethyl-2-phthalimidopyrazine | HCID 13604769 | — |
| 용매 | (Methanesulfinyl)methane--water (1/1) | HCID 23503278 | — |
| 생성물 | 3-Hydroxymethyl-5-dichloromethyl-2-phthalimidopyrazine | HCID 13604777 | 47% |
반응 단계
50 ml of glacial acetic acid and 35 g of potassium acetate were added to a solution of 57.7 g (0.16 mole) of 65% strength 3-chloromethyl-5-dichloromethyl-2-phthalimidopyrazine in 1,000 ml of a 95:5 dimethyl sulfoxide/water mixture. The mixture was stirred for three days at room temperature, after which 1,000 ml of dichloromethane and 1,000 ml of ice-water were added, the resulting mixture was mixed thoroughly and phase separation was effected. The aqueous phase was washed once with 500 ml of dichloromethane and once with 250 ml of dichloromethane, and the combined organic phases were washed twice with 1,000 ml of water, dried over sodium sulfate and evaporated down. The resulting black oil was brought to crystallization with 50 ml of methanol, and then recrystallized from 700 ml of methanol. 16.6 g (47%) of 5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine of melting point 191°-192° C. (sublimation with decomposition) were obtained. 1H-NMR (200 MHz, CDCl3): δ3.3 (t, OH), 4.8 (d, 2H), 6.9 (s, 1H), 8.0 (m, 4H), 9.1 (s, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04725689 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-e68e567d6ece4a128886cf5a849df771 |
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| 출처 메모 | uspto-grants-1988_02 |
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