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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide ester | HCID 76926 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 6-(1-amino-2-oxo-2-phenylethyl)-2-isopropyl-3(2H)-pyridazinone hydrochloride | HCID 69331476 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Tert-butyl (2-{[1-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-2-oxo-2-phenylethyl]amino}-2-oxoethyl)carbamate | HCID 86600908 | 81.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07265120B2 |
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| 출처 데이터셋 | uspto-grants-2007_09 |
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| ORD ID | ord-24b84654b7be4e2794f1aad9976c8871 |
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| 출처 메모 | uspto-grants-2007_09 |
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