3056-18-6

基本信息
2,3,5-三乙酰-2,6-二氯嘌呤核苷
2,3,5-4三乙?;?2,6二氯嘌呤核苷
2,6-二氯嘌呤-2',3',5'-三乙酰
2,6-二氯-2',3',5'-三乙酰基嘌呤核糖苷
9- '2,3,5-三-O-乙?;?Β-D-呋喃核糖基 -2,6-二氯
2,6-二氯-9-(2',3',5'-三-O-乙酰-Β-D-呋喃核糖基)嘌呤
2,6-二氯-9-(2',3',5'-三-O-乙?;?ΒD-呋喃核糖基)嘌呤
2,6-二氯-9-(2',3',5'-三-O-乙?;?BD-呋喃核糖基)嘌呤
9-[2,3,5-三-O-乙酰-BETA-D-呋喃核糖基]-2,6-二氯嘌呤
NSC 76763
2',3',5'-Tri-O-Acetyl-2,6-Dichloropurine
2,6-Dichloro-2',3',5'-triacetyl-purine riboside
9-[2,3,5-tri-O-acetyl--D-ribofuranosyl]-2,6-dichloropurine
9-[2,3,5-TRI-O-ACETYL-SS-D-RIBOFURANOSYL]-2,6-DICHLOROPURINE
9-[2,3,5-TRI-O-ACETYL-BETA-D-RIBOFURANOSYL]-2,6-DICHLOROPURINE
2,6-Dichloro-9-(2’,3’,5’-tri-O-acetyl-β-D-ribofuranosyl)purine
2,6-DICHLORO-9-(2,3,5-TRI-O-ACETYL-B-D-RIBOFURANOSYL)-9H-PURINE
9H-Purine,2,6-dichloro-9-(2,3,5-tri-O-acetyl-b-D-ribofuranosyl)-
物理化學(xué)性質(zhì)
制備方法

16321-99-6

3056-18-6
以(2R,3R,4R,5R)-2-(乙酰氧基甲基)-5-(2-氨基-6-氯-9H-嘌呤-9-基)四氫呋喃-3,4-二基二乙酸酯為原料,合成(2R,3R,4R,5R)-2-(乙酰氧基甲基)-5-(2,6-二氯-9H-嘌呤-9-基)四氫呋喃-3,4-二乙酸二酯的一般步驟如下:將亞硝酸異戊酯(165 g,1.41 mol)溶解于二氯甲烷(500 mL)中,并在0至5°C下攪拌。隨后加入三甲基氯硅烷(76 g,0.70 mol),接著加入化合物IV(100 g,0.234 mol)的二氯甲烷(500 mL)溶液。將混合液滴加至上述反應(yīng)母液中,滴加完畢后,繼續(xù)在相同溫度下攪拌反應(yīng)1小時(shí)。反應(yīng)完成后,加入飽和亞硫酸鈉溶液進(jìn)行淬滅,分液。分離得到的有機(jī)相依次用碳酸氫鈉水溶液和飽和鹽水洗滌,然后用無(wú)水硫酸鈉干燥,過濾。將濾液減壓濃縮至無(wú)餾分蒸出。殘余物通過加入二氯甲烷(100 mL)和正庚烷(350 mL)進(jìn)行重結(jié)晶,得到黃色固體化合物V,即2,6-二氯-9-(2',3',5'-三-O-乙酰基-β-D-呋喃核糖基)嘌呤(86 g,產(chǎn)率82%)。
參考文獻(xiàn):
[1] Journal of Organic Chemistry, 2003, vol. 68, # 2, p. 666 - 669
[2] Canadian Journal of Chemistry, 1981, vol. 59, # 17, p. 2608 - 2611
[3] Patent: CN106397516, 2017, A. Location in patent: Paragraph 0029; 0030; 0080; 0081; 0082; 0083
[4] Journal of Medicinal Chemistry, 1992, vol. 35, # 24, p. 4557 - 4561
[5] Journal of Organic Chemistry, 2002, vol. 67, # 19, p. 6788 - 6796