참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetyl chloride | HCID 6367 | — |
| 반응물 | Vidarabine | HCID 21704 | — |
| 용매 | Dimethylformamide pyridine | HCID 21954950 | — |
| 생성물 | 9-(5-O-acetyl-beta-D-arabinofuranosyl)adenine | HCID 10244806 | — |
반응 단계
To a stirred mixture of 2.67 g. of 9-(β-D-arabinofuranosyl)adenine and 100 ml. of 1:1 dimethylformamide-pyridine is added 0.79 g. of acetyl chloride at 25° C. The mixture is stirred, while being protected from moisture, for 1.5 hours, then treated with 50 g. of crushed ice and evaporated at reduced pressure. The residue is added to a 3× 40 cm. column of dry silica gel and the column is eluted sequentially with 500-ml. portions of 5, 10, 15 and 20% (v/v) methanol in chloroform. Two fractions of eluate (the 15 and 20% methanol in chloroform eluates) are combined and evaporated at reduced pressure to give the desired product 9-(5-O-acetyl-β-D-arabinofuranosyl)adenine; m.p. 197.5°-198.5° C. after crystallization from ethanol, [α]D23 = +23.6° (c = 1% in methanol), λmaxCH3OH = 258 nm (ε = 15,000), water solubility: 9.9 mg./ml.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04069382 |
|---|
| 출처 데이터셋 | uspto-grants-1978_01 |
|---|
| ORD ID | ord-43e6af8678c348f18e9a30af771d5d43 |
|---|
| 출처 메모 | uspto-grants-1978_01 |
|---|