【结 构 式】 |
【分子编号】51335 【品名】2-methyloctanoyl chloride 【CA登记号】 |
【 分 子 式 】C9H17ClO 【 分 子 量 】176.68608 【元素组成】C 61.18% H 9.7% Cl 20.07% O 9.06% |
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:(III)The dilithium anion of octanoic acid (I) was alkylated with iodomethane in the presence of HMPA to afford 2-methyloctanoic acid (II). After conversion of (II) to the corresponding acid chloride (III), condensation with (-)-epigallocatechin (IV) using trifluoroacetic acid as the catalyst furnished the title 3-O-acyl epigallocatechin.
【1】 Uesato, S.; et al.; Antitumor promoting activities of 3-O-acyl-(-)-epigallocatechins. Bioorg Med Chem Lett 2000, 10, 15, 1673. |
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