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【结 构 式】

【分子编号】38236

【品名】4-[(2R)-2-[(1S,3S,5R)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]-2,6-piperidinedione

【CA登记号】66-81-9

【 分 子 式 】C15H23NO4

【 分 子 量 】281.35196

【元素组成】C 64.04% H 8.24% N 4.98% O 22.75%

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)

By condensation of cycloheximide (I) with ethyl 2-bromoacetate (II) by means of K2CO3 and 18-crown-6 in acetone.

1 Grabley, S.; Wyrwa, R.; Schummann, D.; Marsch, S.; Christner, C.; Küllertz, G.; Fischer, G.; Thiericke, R.; Synthesis and cytotoxic evaluation of cycloheximide derivatives as potential inhibitors of FKBP12 with neuroregenerative properties. J Med Chem 1999, 42, 18, 3615.
2 Thiericke, R.; Fischer, G.; Küllertz, G.; Christner, C.; Grabley, S.; Wyrwa, R. (Hans Knöll Institute for Natural Product Research; Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. ); Cyclohexamide derivs. which influence the regeneration of neural tissue. WO 0026188 .
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) 38236 4-[(2R)-2-[(1S,3S,5R)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]-2,6-piperidinedione 66-81-9 C15H23NO4 详情 详情
(II) 16640 Ethyl 2-bromoacetate; Ethyl bromoacetate 105-36-2 C4H7BrO2 详情 详情
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