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HRID 1247798作成日:2026年10月27日

N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide ester → 5-Amino-4-[2-(tert-butoxycarbonylamino)acetyl]amino-1-(2-hydroxyethyl)pyrazole

https://huagongshe.com/reaction/1247798

反応式

関与物質

役割名称HCID仕込み量
反応物N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide esterHCID 76926—
反応物DiisopropylethylamineHCID 81531—
反応物4,5-Diamino-1-(2-hydroxyethyl)pyrazole sulfateHCID 11673148—
溶媒DichloromethaneHCID 6344—
生成物5-Amino-4-[2-(tert-butoxycarbonylamino)acetyl]amino-1-(2-hydroxyethyl)pyrazoleHCID 2190451580.8%

反応手順

To a suspension of 4,5-diamino-1-(2-hydroxyethyl)pyrazole sulfuric acid salt (1.20 g) and N-[2-(tert-butoxycarbonylamino)acetoxy]succinimide (1.35 g) in methylene chloride (20 ml) was added N-ethyldiisopropylamine (2.1 ml) under ice-cooling, and the mixture was stirred at room temperature for 17 hours. The reaction mixture was washed with water (40 ml), saturated aqueous sodium hydrogen carbonate solution (40 ml) and brine (40 ml). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The oily residue was purified by column chromatography on silica gel eluting with 10% methanol/chloroform to give 5-amino-4-[2-(tert-butoxycarbonylamino)acetyl]amino-1-(2-hydroxyethyl)pyrazole (1.20 g) as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07129232B2
出典データセットuspto-grants-2006_10
ORD IDord-52dd1d3126c343a9b2cb3cf6af9914c6
出典メモuspto-grants-2006_10