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2,6-二氯嘌呤核苷的合成工艺研究 被引量:4

Synthesis of 2,6-Dichloroadenosine
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摘要 以2,6-二氯嘌呤和1,2,3,5-四乙酰核糖为原料,四氯化锡为催化剂,130℃下反应18min,得到中间体2,6-二氯嘌呤-2',3',5'-三乙酰基核苷。该中间体在硫酸-甲醇中脱酰基得到2,6-二氯嘌呤核苷,为白色粉状结晶,收率63%,纯度(HPLC)≥99.0%,熔点152 ̄154℃。 A new method for synthesizing 2,6-dichloroadenosine was reported in the paper. The starting material 2,6- dichloropurine was condensed with 1,2,3,5-tetraacetylribofuranose at 130℃ for 18 minutes to form 2', 3', 5'-triacetyl- 2,6-dichloroadenosine, which was deprotected in H2SO4-CH3OH at 0 -5℃ to give the target product 2,6- dichloroadenosine as a white crystalline powder. The yield was 63%, purity (HPLC) ≥ 99.0%, and the melting point of the product was 152-154℃.
出处 《精细化工中间体》 CAS 2007年第3期35-37,共3页 Fine Chemical Intermediates
基金 国家自然科学基金资助项目(20372018)。
关键词 2 6-二氯嘌呤核苷 2 6-二氯嘌呤 1 2 3 5-四乙酰基核糖 2,6-dichloroadenosine 2,6-dichloropurine 1,2,3,5-tetraacetylribofuranose
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同被引文献34

  • 1周乐,史远刚,王建辰.6-氯-9-β-D-呋喃核糖嘌呤的合成[J].化学通报,1996(5):31-32. 被引量:5
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