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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 619441생성일: 2026년 10월 25일

N-(tert-Butoxycarbonyl)-1,5-diaminopentane → 4,5-Dihydro-4[5-(tert-butoxycarbonylamino)pentan-1-yl]-3H-1,4,8b-triazaacenaphthylen-5-one

https://huagongshe.com/reaction/619441

반응식

참여 물질

역할이름HCID투입량
반응물N-(tert-Butoxycarbonyl)-1,5-diaminopentaneHCID 4352—
반응물TriethylamineHCID 8471—
반응물3-[(Trimethylammonio)methyl]-5-ethoxycarbonylimidazo[1,2-a]pyridine iodideHCID 21190128—
생성물4,5-Dihydro-4[5-(tert-butoxycarbonylamino)pentan-1-yl]-3H-1,4,8b-triazaacenaphthylen-5-oneHCID 2119017354.8%

반응 단계

A solution of 7.78 g (20 mmol) of 3-[(trimethylammonio)methyl]-5-ethoxycarbonylimidazo [1,2-a]pyridine iodide, 6.07 g (30 mmol) of 5-tert-butoxycarbonylamino-1-pentylamine and 5.58 ml (40 mmol) of triethylamine was heated for 64 hours under reflux. The solvent was distilled off. To the residue was added methylene chloride, washed with water, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by column chromatography (eluent: ethyl acetate/ethanol=10:1) to afford 3.93 g of the desired compound (54.9%, a pale yellow solid).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05958942
출처 데이터셋uspto-grants-1999_09
ORD IDord-fe3959d2b56d42c4b63412223c5abdc6
출처 메모uspto-grants-1999_09