Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1057514생성일: 2026년 10월 27일
Diisopropylethylamine → methyl 2-{8-chloro-2-[N-(3-(1,2,3,4-tetrahydropyridino[2,3-b]pyridin-7-yl)propyl)carbamoyl]-1H,3H,4H,5H-benzo[e]azepin-5-yl}acetate
https://huagongshe.com/reaction/1057514
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 3-(5,6,7,8-Tetrahydro-1,8-naphthyridin-2-yl)propan-1-amine | HCID 9877599 | — |
| 반응물 | Phosgen toluene | HCID 19083224 | — |
| 반응물 | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| 생성물 | methyl 2-{8-chloro-2-[N-(3-(1,2,3,4-tetrahydropyridino[2,3-b]pyridin-7-yl)propyl)carbamoyl]-1H,3H,4H,5H-benzo[e]azepin-5-yl}acetate | HCID 69157953 | — |
반응 단계
A solution of methyl 2-{2-[(tert-butyl)oxycarbonyl-8-chloro-1H,3H,4H,5H-benzo[e]azepin-5-yl}acetate (1 eq) in 1.17 M of HCl/ethyl acetate (30 eq) was stirred at room temperature for 18 hr. The reaction mixture was concentrated and dried under vacuum oven. The resulting residue was dissolved in methylene chloride (0.15 M) and followed by the addition of phosgene/toluene (20%) (10 eq) under nitrogen. After stirring for 1 hr, the solvent was removed by rotary evaporation. The residue was dissolved in 1 ml of N,N-dimethylformamide (0.07 M), followed by the addition of 3-(1,2,3,4-tetrahydropyridino[2,3-b]pyridin-7-yl)propylamine (2 eq) and N,N-diisopropylethylamine (10 eq). The reaction mixture was heated at 50° C. for 2 hr. The reaction solvent was removed by rotary evaporation and the residue was purified by flash chromatography (5% methanol/methylene chloride. EI-MS m/z 471 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06514964B1 |
|---|
| 출처 데이터셋 | uspto-grants-2003_02 |
|---|
| ORD ID | ord-72527742638549a38e123850f576bf01 |
|---|
| 출처 메모 | uspto-grants-2003_02 |
|---|