Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetic acid (2R,3R,4R,5R)-3,4-diacetoxy-5-(6-chloro-2-iodo-purin-9-YL)-tetrahydro-furan-2-ylmethyl ester → 2-Iodoadenosine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetic acid (2R,3R,4R,5R)-3,4-diacetoxy-5-(6-chloro-2-iodo-purin-9-YL)-tetrahydro-furan-2-ylmethyl ester | HCID 482588 | — |
| 반응물 | Ammonia methanol | HCID 21705897 | — |
| 생성물 | 2-Iodoadenosine | HCID 169662 | 90% |
반응 단계
6.0 g of 6-chloro-2-iodo-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)purine was added to 60 ml of methanol/ammonia (saturated at 0° C.) to cause reaction at a temperature of 60° C. for 17 hours in a sealed tube. The reaction solution was cooled, then degassed, and concentrated under reduced pressure. Crystallization of the residue from water afforded 3.94 g of 2-iodoadenosine (90% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05270304 |
| 출처 데이터셋 | uspto-grants-1993_12 |
| ORD ID | ord-ee01eded22734121b23cb3a8d04cef6f |
| 출처 메모 | uspto-grants-1993_12 |