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【结 构 式】

【分子编号】19023

【品名】(1R,4S)-2-Methyl-4-[4-(3-methyl-2-butenyloxy)benzylidene]dispiro[2,5-diazabicyclo[3,2,1]octane-6,1'-cyclohexane-4',2''-[1,3]-dioxolane]

【CA登记号】

【 分 子 式 】C26H36N2O3

【 分 子 量 】424.58352

【元素组成】C 73.55% H 8.55% N 6.6% O 11.3%

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:(XIX)

Mesylation of either isomer, followed by elimination in mesylate (XVII) with potassium tert-butoxide gave enone (XVIII). Reduction of carbonyl group was then effected with AlH3, prepared from lithium aluminum hydride and aluminum chloride yielding (XIX), and finally, deprotection of acetal (XIX) with HCl in acetone afforded the desired compound.

1 Nagumo, S.; et al.; Total synthesis of antimuscarinic alkaloid, (±)-TAN1251A. Tetrahedron 2002, 58, 24, 4917.
2 Nagumo, S.; et al.; Total synthesis of (±)-TAN1251A. Tetrahedron Lett 1998, 39, 25, 4493.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(XVI) 19020 (1R,4S)-4-[1-Hydroxy-1-[4-(3-methyl-2-butenyloxy)phenyl]methyl]-2-methyldispiro[2,5-diazabicyclo[3,2,1]octane-6,1'-cyclohexane-4',2''-[1,3]-dioxolan]-3-one C26H36N2O5 详情 详情
(XVII) 19021 (1R,4S)-4-[1-(Methanesulfonyloxy)-1-[4-(3-methyl-2-butenyloxy)phenyl]methyl]-2-methyldispiro[2,5-diazabicyclo[3,2,1]octane-6,1'-cyclohexane-4',2''-[1,3]-dioxolan]-3-one C27H38N2O7S 详情 详情
(XVIII) 19022 (1R,4S)-2-Methyl-4-[4-(3-methyl-2-butenyloxy)benzylidene]dispiro[2,5-diazabicyclo[3,2,1]octane-6,1'-cyclohexane-4',2''-[1,3]-dioxolan]-3-one C26H34N2O4 详情 详情
(XIX) 19023 (1R,4S)-2-Methyl-4-[4-(3-methyl-2-butenyloxy)benzylidene]dispiro[2,5-diazabicyclo[3,2,1]octane-6,1'-cyclohexane-4',2''-[1,3]-dioxolane] C26H36N2O3 详情 详情
Extended Information