Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N-(tert-Butoxycarbonyl)-1,5-diaminopentane → 4,5-Dihydro-4[5-(tert-butoxycarbonylamino)pentan-1-yl]-3H-1,4,8b-triazaacenaphthylen-5-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N-(tert-Butoxycarbonyl)-1,5-diaminopentane | HCID 4352 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 3-[(Trimethylammonio)methyl]-5-ethoxycarbonylimidazo[1,2-a]pyridine iodide | HCID 21190128 | — |
| 생성물 | 4,5-Dihydro-4[5-(tert-butoxycarbonylamino)pentan-1-yl]-3H-1,4,8b-triazaacenaphthylen-5-one | HCID 21190173 | 54.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05958942 |
| 출처 데이터셋 | uspto-grants-1999_09 |
| ORD ID | ord-fe3959d2b56d42c4b63412223c5abdc6 |
| 출처 메모 | uspto-grants-1999_09 |