tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate -Drug Synthesis Database

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【结构式】

【分子编号】66779

【品名】tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate

【CA登记号】　

【分子式】C₁₃H₁₈O₉

【分子量】318.28052

【元素组成】C 49.06% H 5.7% O 45.24%

与该中间体有关的原料药合成路线共 1 条

合成路线1

合成路线1

该中间体在本合成路线中的序号：(II)

　

参考文献中间体

【1】 Storer R. Moussa A. Wang JY. et al. 2005. Synthesis of β-L-2-deoxy-nucleosides from furanoses and pyranoses via a chloro-sugar and anhydro-l-furanosyl-nucleobase intennediatcs as potential antiviral and antineoplastic agents. W0 2005003374

中间体序号	中间体编号	品名	CAS号	分子式	供应商	用于合成
（X）	62918	{(2S,3R,5S)-3-[(4-methylbenzoyl)oxy]-5-[5-methyl-2,4-dioxo-3,4-dihydro-1(2H)-pyrimidinyl]tetrahydro-2-furanyl}methyl 4-methylbenzoate		C₂₆H₂₆N₂O₇	详情	详情
(I)	17520	(3R,4S,5S)tetrahydro-2H-pyran-2,3,4,5-tetrol; L-(+)-Arabinose	7296-56-2	C₅H₁₀O₅	详情	详情
(II)	66779	tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate		C₁₃H₁₈O₉	详情	详情
(III)	20353	(2S,3R,4S,5S)-3,5-bis(acetoxy)-2-bromotetrahydro-2H-pyran-4-yl acetate		C₁₁H₁₅BrO₇	详情	详情
(IV)	54162	(3S,4R)-3-(acetyloxy)-3,4-dihydro-2H-pyran-4-yl acetate	n/a	C₉H₁₂O₅	详情	详情
(V)	66780	3,4-dihydro-2H-pyran-3,4-diol		C₅H₈O₃	详情	详情
(VI)	12241	(2R,3S)-2-(Hydroxymethyl)-5-methoxytetrahydro-3-furanol		C₆H₁₂O₄	详情	详情
(VII)	62915	{(2S,3R)-5-methoxy-3-[(4-methylbenzoyl)oxy]tetrahydro-2-furanyl}methyl 4-methylbenzoate		C₂₂H₂₄O₆	详情	详情
(VIII)	37194	(2R,3S)-5-Chloro-2-[[(4-methylbenzoyl)oxy]methyl]tetrahydro-3-furanyl 4-methylbenzoate	4330-21-6	C₂₁H₂₁ClO₅	详情	详情
(IX)	12204	5-Methyl-2,4(1H,3H)-pyrimidinedione; Thymine	65-71-4	C₅H₆N₂O₂	详情	详情

Extended Information