((2R,4R)-2-((((9H-fluoren-9-yl)peroxy)carbonyl)oxy)-4-(4-amino-2-oxo-1,3,5-triazin-1(2H)-yl)cyclopentyl)methyl 9H-fluoren-9-yl carbonoperoxoate -Drug Synthesis Database

【结构式】

【分子编号】66257

【品名】((2R,4R)-2-((((9H-fluoren-9-yl)peroxy)carbonyl)oxy)-4-(4-amino-2-oxo-1,3,5-triazin-1(2H)-yl)cyclopentyl)methyl 9H-fluoren-9-yl carbonoperoxoate

【CA登记号】　

【分子式】C₃₇H₃₀N₄O₉

【分子量】674.667

【元素组成】C 65.87% H 4.48% N 8.30% O 21.34%

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：(V)

【1】 BerrHattar J, Jiricny J. 1986. An improved syntbesis of 2'-deoxy5-azacytidine by condensation of an 9-flu-orenylmethoxycarbonyl-protected sug:ar onto the silylated base. J Org Chem, 51r 3211 --3213

中间体序号	中间体编号	品名	分子式	供应商	用于合成
(I)	66254	(3S,5S)-2-(hydroxymethyl)-5-methoxytetrahydrofuran-3-ol	C₆H₁₂O₄	详情	详情
(II)	66255	((2S,4S)-2-((((9H-fluoren-9-yl)peroxy)carbonyl)oxy)-4-methoxycyclopentyl)methyl 9H-fluoren-9-yl carbonoperoxoate	C₃₅H₃₀O₉	详情	详情
(III)	66256	((1R,4R)-2-((((9H-fluoren-9-yl)peroxy)carbonyl)oxy)-4-chlorocyclopentyl)methyl 9H-fluoren-9-yl carbonoperoxoate	C₃₄H₂₇ClO₈	详情	详情
(IV)	11626	N-(Trimethylsilyl)-4-[(trimethylsilyl)oxy]-1,3,5-triazin-2-amine; N-(Trimethylsilyl)-N-[4-[(trimethylsilyl)oxy]-1,3,5-triazin-2-yl]amine	C₉H₂₀N₄OSi₂	详情	详情
(V)	66257	((2R,4R)-2-((((9H-fluoren-9-yl)peroxy)carbonyl)oxy)-4-(4-amino-2-oxo-1,3,5-triazin-1(2H)-yl)cyclopentyl)methyl 9H-fluoren-9-yl carbonoperoxoate	C₃₇H₃₀N₄O₉	详情	详情
(VI)	66142		C₃₇H₃₀N₄O₉	详情	详情

Extended Information