Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HCID 54512598, 화합물 → (R)-2-oxo-3-tert-butoxycarbonylamino-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | HCID 54512598 | HCID 54512598 | — |
| 촉매 | HCID 178418390 | HCID 178418390 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (R)-2-oxo-3-tert-butoxycarbonylamino-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine | HCID 12988641 | 80% |
반응 단계
10% palladium carbon (1 g) was added to a solution of (R)-(−)-2-tert-butoxycarbonylamino-3-(2-nitrophenylamino)propionic acid (7.6 g) in tetrahydrofuran (100 ml), and the mixture was stirred under hydrogen atmosphere at room temperature for 3 hours. The reaction mixture was filtrated, and the filtrate was concentrated under reduced pressure, to thereby obtain (R)-2-tert-butoxycarbonylamino-3-(2-aminophenylamino)propionic acid. The residue was dissolved in toluene (100 ml), the solution was refluxed overnight. After allowed to cool, the reaction mixture was concentrated under reduced pressure, the residue was purified by silica gel column chromatography(ethyl acetate:n-hexane=1:1), to thereby obtain 5.16 g of the title compound (Yield 80%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06239131B1 |
| 출처 데이터셋 | uspto-grants-2001_05 |
| ORD ID | ord-687427fe6fb64bada85a3d4ab6f4e89d |
| 출처 메모 | uspto-grants-2001_05 |