2-((4-methoxybenzyl)oxy)-2-phenethylpentan-1-ol -Drug Synthesis Database

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【结构式】

【分子编号】66870

【品名】2-((4-methoxybenzyl)oxy)-2-phenethylpentan-1-ol

【CA登记号】　

【分子式】C₂₁H₂₈O₃

【分子量】328.45152

【元素组成】C 76.79% H 8.59% O 14.61%

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：(X)

　

参考文献中间体

【1】 Trost BM, Andersen NG. 2002. Utilization of molybdenum-and palladium-catalyzed dynamic kinetic asymmetric transformations for the preparation of tertiary and quatemary stereogenic centers; a concise synthesis of tipranavir. J Am Chem Soc, 124 (48): 14320～14321

中间体序号	中间体编号	品名	CAS号	分子式	供应商	用于合成
(IV)	66865	methyl 3-(3-nitrophenyl)pent-4-enoate		C₁₂H₁₃NO₄	详情	详情
(V)	16524	bromo(vinyl)magnesium	1826-67-1	C₂H₃BrMg	详情	详情
(VII)	66867	1-propyl-1-vinylcyclopropane		C₈H₁₄	详情	详情
(IX)	66869	(E)-2-((4-methoxybenzyl)oxy)-2-styrylpentan-1-ol		C₂₁H₂₆O₃	详情	详情
(XII)	66872	(5S)-methyl 5-((4-methoxybenzyl)oxy)-2-((R)-1-(3-nitrophenyl)allyl)-3-oxo-5-phenethyloctanoate		C₃₄H₃₉NO₇	详情	详情
(XIII)	66873	(5S)-methyl 5-hydroxy-2-((R)-1-(3-nitrophenyl)allyl)-3-oxo-5-phenethyloctanoate		C₂₆H₃₁NO₆	详情	详情
(XIV)	66874	(S)-4-hydroxy-3-((R)-1-(3-nitrophenyl)allyl)-6-phenethyl-6-propyl-5,6-dihydro-2H-pyran-2-one		C₂₅H₂₇NO₅	详情	详情
(XV)	21168	(6R)-4-hydroxy-3-[(1R)-1-(3-nitrophenyl)propyl]-6-phenethyl-6-propyl-5,6-dihydro-2H-pyran-2-one		C₂₅H₂₉NO₅	详情	详情
(I)	66862	1-(3-nitrophenyl)prop-2-en-1-ol		C₉H₉NO₃	详情	详情
(II)	66863	tert-butyl (1-(3-nitrophenyl)allyl) carbonate		C₁₄H₁₇NO₅	详情	详情
(III)	66864	dimethyl 2-(1-(3-nitrophenyl)allyl)malonate		C₁₄H₁₅NO₆	详情	详情
(VI)	66866	1-chloropentan-2-one		C₅H₉ClO	详情	详情
(VIII)	66868	2-((4-methoxybenzyl)oxy)-2-vinylpentan-1-ol		C₁₅H₂₂O₃	详情	详情
(X)	66870	2-((4-methoxybenzyl)oxy)-2-phenethylpentan-1-ol		C₂₁H₂₈O₃	详情	详情
(XI)	66871	1-methoxy-4-(((3-phenethylhex-1-en-3-yl)oxy)methyl)benzene		C₂₂H₂₈O₂	详情	详情
(XVI)	66879	2-((4-methoxybenzyl)oxy)-2-phenethylpentanal		C₂₁H₂₆O₃	详情	详情

Extended Information