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HRID 915016作成日:2026年10月26日

N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide ester → Tert-butyl (2-{[1-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-2-oxo-2-phenylethyl]amino}-2-oxoethyl)carbamate

https://huagongshe.com/reaction/915016

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6-(1-amino-2-oxo-2-phenylethyl)-2-isopropyl-3(2H)-pyridazinone hydrochlorideHCID 69331476—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl (2-{[1-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-2-oxo-2-phenylethyl]amino}-2-oxoethyl)carbamateHCID 8660090881.2%

反応条件

温度22.5 °C

反応手順

Under ice-cooling, to a suspension of 6-(1-amino-2-oxo-2-phenylethyl)-2-isopropyl-3(2H)-pyridazinone hydrochloride (1.00 g) and tert-butyl {2-[(2,5-dioxo-1-pyrrolidinyl)oxy]-2-oxoethyl}carbamate (973 mg) in CH2Cl2 (10 ml) was added ethyl(diisopropyl)amine (0.651 ml) and stirred at the same temperature for 2 hours and at 20-25° C. for 18 hours. The mixture was washed with water, dried over MgSO4 and concentrated under reduced pressure to give syrup. The syrup was purified by column chromatography on silica gel (EtOAc only) to give tert-butyl (2-{[1-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-2-oxo-2-phenylethyl]amino}-2-oxoethyl)carbamate as an amorphous solid (1.13 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07265120B2
出典データセットuspto-grants-2007_09
ORD IDord-24b84654b7be4e2794f1aad9976c8871
出典メモuspto-grants-2007_09