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HRID 1653683作成日:2026年10月27日

Dimethylformamide → methyl N(alpha)-[4-[2-(2,4-diamino-7H-pyrrolo[2,3-d]pyrimidin-5-yl)ethyl]benzoyl]-N-(delta)-(t-butyloxycarbonyl)-L-ornithinate

https://huagongshe.com/reaction/1653683

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Diethyl cyanophosphonateHCID 76257—
反応物(2S)-2-amino-5-(((tert-butoxy)carbonyl)amino)pentanoic acidHCID 6993436—
反応物4-[2-(2,4-diamino-7H-pyrrolo [2,3-d]pyrimidin-5-yl)ethyl]benzoic acidHCID 10447331—
溶媒TriethylamineHCID 8471—
生成物methyl N(alpha)-[4-[2-(2,4-diamino-7H-pyrrolo[2,3-d]pyrimidin-5-yl)ethyl]benzoyl]-N-(delta)-(t-butyloxycarbonyl)-L-ornithinateHCID 1060217785%

反応手順

To a DMF solution of 4-[2-(2,4-diamino-7H-pyrrolo [2,3-d]pyrimidin-5-yl)ethyl]benzoic acid (1.52 g) and methyl ester of N(δ)-t-butyloxycarbonyl-L-ornithine (1.3 g) was added diethyl cyanophosphate (1.4 g). The mixture was stirred for one hour at room temperature in the presence of triethylamine (3.0 g). The reaction mixture was concentrated under reduced pressure. The concentrate was purified by column chromatography on silica gel (carrier: 30 g; chloroform:ethanol containing 1% ammonium=20:1-15:1) to afford methyl N(α)-[4-[2-(2,4-diamino-7H-pyrrolo[2,3-d]pyrimidin-5-yl)ethyl]benzoyl]-N-(δ)-(t-butyloxycarbonyl)-L-ornithinate (2.30 g; yield 85%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05403843
出典データセットuspto-grants-1995_04
ORD IDord-6c87443a3ce54b5fa4461fbfe227b526
出典メモuspto-grants-1995_04