Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetic Anhydride → 3'-Azido-2',3'-dideoxy-5-bromouridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Bromine | HCID 24408 | — |
| 반응물 | Navuridine | HCID 55262 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 3'-Azido-2',3'-dideoxy-5-bromouridine | HCID 64978 | — |
반응 단계
3'-Azido-5-bromo-2',3'-dideoxyuridine was prepared from the known 3'-azido-2',3'-dideoxyuridine (T. A. Krenitsky, et al., J. Med. Chem., 26, 891, (1983)) (0.827 g, 3.3 mMol) by first acetylating the 5'-hydroxyl group with acetic anhydride (15 mL) then by brominating the 5 position by the addition of acetic acid (0.5 mL) and bromine (0.566 g). The red-brown solution was stirred at room temperature for two hours. The reaction was taken to an oil in vacuo and triturated with ethyl ether. The oil was dissolved in methanol ammonia to remove the acetyl group. The desired product was isolated by chromatography on silica gel by elution with CHCl3 :MeOH (95:5 v/v). The yield was 32%; mp=148°-149° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05064946 |
| 출처 데이터셋 | uspto-grants-1991_11 |
| ORD ID | ord-37707a9b32a64b05be2a81c10c953f47 |
| 출처 메모 | uspto-grants-1991_11 |