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【结 构 式】

【分子编号】27915

【品名】(2R,3S,4S,5R)-2-[4-amino-2-oxo-1(2H)-pyrimidinyl]-4-hydroxy-5-(hydroxymethyl)tetrahydro-3-furancarbonitrile

【CA登记号】

【 分 子 式 】C10H12N4O4

【 分 子 量 】252.22984

【元素组成】C 47.62% H 4.8% N 22.21% O 25.37%

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:(I)

CS-682 has been synthesized by several related ways: 1) By acylation of 2'-cyano-2'-deoxy-1-(beta-D-arabinofuranosyl)cytosine (I) with hexadecanoyl chloride (II) and trimethylsilyl chloride in pyridine. 2) By acylation of 2'-cyano-2'-deoxy-1-(beta-D-arabinofuranosyl)cytosine (I) with hexadecanoyl anhydride (III) in hot DMF. 3) The protection of the OH groups of 2'-cyano-2'-deoxy-1-(beta-D-arabinofuranosyl)cytosine (I) with 1,3-dichloro-1,1,3,3-tetraisopropyldisiloxane in pyridine gives the 3',5'-cyclic disiloxane (IV), which is acylated by means of hexadecanoic acid (V) and DCC in THF, yielding the silylated compound (VI). Finally, this compound is deprotected with tetrabutylammonium fluoride (TBAF) in acetic acid.

1 Castaner, J.; Hoshi, A.; CS-682. Drugs Fut 1999, 24, 9, 957.
2 Kaneko, M.; Hotoda, H.; Shibata, T.; Kobayashi, T.; Mitsuhashi, Y.; Matsuda, A.; Sasaki, T. (Sankyo Co., Ltd.); Pyrimidine nucleoside derivs. having anti-tumor activity, their preparation and use. EP 0536936; JP 1993194497; US 5691319 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 27915 (2R,3S,4S,5R)-2-[4-amino-2-oxo-1(2H)-pyrimidinyl]-4-hydroxy-5-(hydroxymethyl)tetrahydro-3-furancarbonitrile C10H12N4O4 详情 详情
(II) 16480 Palmitoyl Chloride; hexadecanoyl chloride 112-67-4 C16H31ClO 详情 详情
(III) 27916 hexadecanoic anhydride 623-65-4 C32H62O3 详情 详情
(IV) 27917 (6aR,8R,9S,9aS)-8-[4-amino-2-oxo-1(2H)-pyrimidinyl]-2,2,4,4-tetraisopropyltetrahydro-6H-furo[3,2-f][1,3,5,2,4]trioxadisilocine-9-carbonitrile C22H38N4O5Si2 详情 详情
(V) 27918 palmitic acid 57-10-3 C16H32O2 详情 详情
(VI) 27919 N-[1-[(6aR,8R,9S,9aS)-9-cyano-2,2,4,4-tetraisopropyltetrahydro-6H-furo[3,2-f][1,3,5,2,4]trioxadisilocin-8-yl]-2-oxo-1,2-dihydro-4-pyrimidinyl]hexadecanamide C38H68N4O6Si2 详情 详情
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