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HRID 431753作成日:2026年10月26日

Imidazole → cis4-(tert-butyldimethylsilyloxy)-N-benzyloxycarbonyl-D-proline

https://huagongshe.com/reaction/431753

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物(2R,4R)-1-((benzyloxy)carbonyl)-4-hydroxypyrrolidine-2-carboxylic acidHCID 688416—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl acetate hexaneHCID 21226206—
生成物cis4-(tert-butyldimethylsilyloxy)-N-benzyloxycarbonyl-D-prolineHCID 6999564189.5%

反応手順

To a mixture of cis4-hydroxy-N-benzyloxycarbonyl-D-proline (18.74 g) and imidazole (11.56 g) in DMF (100 mL) was added TBDMSCl (23.36 g) at 5° C. After stirring at room temperature for 16 hours, the reaction mixture was diluted with EtOAc-hexane (1:1, 600 mL), washed with 1N HCl, water and brine, dried (MgSO4), and evaporated in vacuo. The residue was dissolved in MeOH-THF (3:1, 400 mL). To the solution was added an aqueous solution (100 mL) of K2CO3 (9.77 g) at 5° C., and the mixture was stirred at the same temperature for 1 hour. The organic solvent was evaporated, and the residue was adjusted to pH 2 by the addition of 3N HCl, and extracted with EtOAc. The organic layer was washed with water and brine, dried (MgSO4), and evaporated in vacuo. The residue was purified by silica gal column chromatography to give cis-4-(tert-butyldimethylsilyloxy)-N-benzyloxycarbonyl-D-proline (23.99 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06660759B1
出典データセットuspto-grants-2003_12
ORD IDord-ce1db149d5d3404ab6fb24f15fa37f3a
出典メモuspto-grants-2003_12