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【结 构 式】

【分子编号】37193

【品名】1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-5-(hydroxymethyl)-2,4(1H,3H)-pyrimidinedione

【CA登记号】

【 分 子 式 】C10H14N2O6

【 分 子 量 】258.23104

【元素组成】C 46.51% H 5.46% N 10.85% O 37.17%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(VI)

The reaction of 1-(2-deoxy-beta-D-ribofuranosyl)uracil (V) with CH2O and KOH gives 1-(2-deoxy-beta-D-ribofuranosyl)-5-hydroxymethyluracil (VI), which is treated with methanolic-HCl. Chromatography on silica gel yields the target compound.

1 Gupta, V.S.; Bubbar, G.L.; Synthesis of 5-substituted ether derivatives of 5-hydroxymethyl deoxyuridine and their 'alpha-anomers'. Can J Chem 1970, 48, 20, 3147.
2 Gupta, V.S.; Methoxymethyl-2'-deoxyuridine. Drugs Fut 1981, 6, 1, 32.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(V) 11875 1-[(2R,4S,5R)-4-Hydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-2,4(1H,3H)-pyrimidinedione; 2'-Deoxyuridine 951-78-0 C9H12N2O5 详情 详情
(VI) 37193 1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-5-(hydroxymethyl)-2,4(1H,3H)-pyrimidinedione C10H14N2O6 详情 详情
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