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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 915016생성일: 2026년 10월 26일

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

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참여 물질

역할이름HCID투입량
반응물N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide esterHCID 76926—
반응물DiisopropylethylamineHCID 81531—
반응물6-(1-amino-2-oxo-2-phenylethyl)-2-isopropyl-3(2H)-pyridazinone hydrochlorideHCID 69331476—
용매DichloromethaneHCID 6344—
생성물Tert-butyl (2-{[1-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-2-oxo-2-phenylethyl]amino}-2-oxoethyl)carbamateHCID 8660090881.2%

반응 조건

온도22.5 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07265120B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-24b84654b7be4e2794f1aad9976c8871
출처 메모uspto-grants-2007_09