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Ethanesulfonic acid → 9-(1,3-Diacetoxy-2-propoxymethyl)-2-acetamido-6-chloropurine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethanesulfonic acid | HCID 11668 | — |
| 反応物 | 1,3-Propanediol, 2-((acetyloxy)methoxy)-, 1,3-diacetate | HCID 9794888 | — |
| 反応物 | HCID 178474411 | HCID 178474411 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 9-(1,3-Diacetoxy-2-propoxymethyl)-2-acetamido-6-chloropurine | HCID 14855154 | 23.7% |
反応手順
A round-bottomed flask (10 ml) was charged with N-acetyl-2-acetamido-6-chloropurine (2.0 g, 7.9 mmoles), 1,3-diacetoxy-2-propoxymethyl acetate (2.7 g, 10.9 mmoles), and ethanesulfonic acid (63 mg). The mixture was heated in an oil bath maintained at 130° and a vacuum was applied. Thin layer chromatography showed no heterocyclic starting material after 1.5 hours and heating was discontinued. The mixture was dissolved in dichloromethane (50 ml) and filtered through Celite. The filtrate was evaporated to a residue and chromatographed on silica gel using dichloromethane/methanol (98:2) as the eluant. The product-containing fractions were combined and evaporated to give 0.75 g of pure product, m.p. 139°-140°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04897479 |
| 出典データセット | uspto-grants-1990_01 |
| ORD ID | ord-0343305172d346339c8b2788ac7ef181 |
| 出典メモ | uspto-grants-1990_01 |