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HRID 901475作成日:2026年10月25日

Ethylene Oxide → 1-(2-Hydroxy-ethyl)-4-pentyl-pyrrolidine-2-carboxylic acid [2-methyl-1-(3,4,5-trihydroxy-6-propyl-tetrahydro-pyran-2-yl)-propyl]-amide

https://huagongshe.com/reaction/901475

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene OxideHCID 6354—
反応物4-Pentyl-pyrrolidine-2-carboxylic acid [2-methyl-1-(3,4,5-trihydroxy-6-propyl-tetrahydro-pyran-2-yl)-propyl]-amideHCID 11223736—
溶媒MethanolHCID 887—
溶媒Diethyl EtherHCID 3283—
生成物1-(2-Hydroxy-ethyl)-4-pentyl-pyrrolidine-2-carboxylic acid [2-methyl-1-(3,4,5-trihydroxy-6-propyl-tetrahydro-pyran-2-yl)-propyl]-amideHCID 1131708134%

反応手順

The title compound was prepared according to the process illustrated in Scheme 19. Ethylene oxide was used as the alkylating agent. To a stirred solution of 4-Pentyl-pyrrolidine-2-carboxylic acid [2-methyl-1-(3,4,5-trihydroxy-6-propyl-tetrahydro-pyran-2-yl)-propyl]-amide (example 103) (12.0 mg 0.029 mmol, 1 equiv) and TEA (100 μL) in MeOH (2 mL) at 0° C. was added condensed ethylene oxide (200 μL) was added and the reaction mixture stirred 48 h. The reaction mixture evaporated to dryness, and the resulting residue was purified by column chromatography on silica 20% 0.25M NH3 in MeOH/DCM to give the crude N alkylated product. The crude product was taken up in Et2O, filtered and the filtrate treated with 2M HCl in Et2O, the precipitated HCl salt was collected washed with Et2O and lyophilized to give the title compound as a colorless powder (4.4 mg 34%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07361743B2
出典データセットuspto-grants-2008_04
ORD IDord-22bc6d21f833445f992e47c5038a1d43
出典メモuspto-grants-2008_04