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HRID 590885作成日:2026年10月26日

Imidazole → Methyl (S)-2-(3-(3-(bis(4-methoxybenzyl)amino)-1-trityl-1H-pyrazolo[4,3-c]pyridin-6-yl)ureido)-2-phenylacetate

https://huagongshe.com/reaction/590885

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物DiisopropylethylamineHCID 81531—
反応物Methyl phenylglycinate, L-HCID 1201451—
反応物3-N,N-bis(4-methoxybenzyl)-1-trityl-1H-pyrazolo[4,3-c]pyridine-3,6-diamineHCID 118272377—
溶媒1,4-DioxaneHCID 31275—
生成物Methyl (S)-2-(3-(3-(bis(4-methoxybenzyl)amino)-1-trityl-1H-pyrazolo[4,3-c]pyridin-6-yl)ureido)-2-phenylacetateHCID 131734504—

反応手順

To a solution of 3-N,N-bis(4-methoxybenzyl)-1-trityl-1H-pyrazolo[4,3-c]pyridine-3,6-diamine (0.1 g, 0.16 mmol) in anhydrous 1,4-dioxane (3 mL) was added CDI (0.13 g, 0.79 mmol) followed by the addition of imidazole (0.05 g, 0.78 mmol) and the contents were stirred at ambient temperature. After 16 h, DIPEA (0.12 mL, 0.64 mmol) and (S)-methyl-2-amino-2-phenylacetate (0.064 g, 0.32 mmol) were added and stirred. After 2 h, the reaction mixture was quenched with H2O and the organic contents were extracted with EtOAc (2×20 mL), dried over anhydrous Na2SO4 and concentrated. The residue thus obtained was purified by preparative HPLC to afford the title compound MS ES calc'd. for C51H46N6O5 [M+H]+ 823. Found 823.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09233979B2
出典データセットuspto-grants-2016_01
ORD IDord-a1a7e7a2af0941cfbae85fcd17e75210
出典メモuspto-grants-2016_01