Hydrochloric Acid → 9-Bromo-10-fluoro-3,4,7,8-tetrahydro-[1,4]diazepino[7,1-a]isoquinoline-2,5-dione
반응식
[Br:1][C:2]1[C:11]([F:12])=[CH:10][CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][N:6]([C:18](=[O:28])[CH2:19][NH:20][C:21](OC(C)(C)C)=[O:22])[CH:7]2[CH2:13]C(OC)=O.BrC1C(F)=CC=C2C=1CCNC2CC(OC)=O.C(NCC(O)=O)(OC(C)(C)C)=O.C(N(CC)CC)C.Cl>CCOC(C)=O.C(P1(=O)OP(CCC)(=O)OP(CCC)(=O)O1)CC>[Br:1][C:2]1[C:11]([F:12])=[CH:10][CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][N:6]1[C:18](=[O:28])[CH2:19][NH:20][C:21](=[O:22])[CH:13]=[C:7]12참가 물질
반응물 5
생성물 1
시약·촉매·용매 2
실험 절차
methyl 2-(5-bromo-2-(2-((tert-butoxycarbonyl)amino)acetyl)-6-fluoro-1,2,3,4-tetrahydroisoquinolin-1-yl)acetate. To a stirred solution of methyl 2-(5-bromo-6-fluoro-1,2,3,4-tetrahydroisoquinolin-1-yl)acetate (41.58 g, 138 mmol), Boc-glycine (26.5 g, 151 mmol) and triethylamine (38.4 mL, 275 mmol) in AcOEt (690 mL), T3P (98 mL, 165 mmol, 50% m/m in AcOEt) was added and the solution was stirred at RT for 1 h. 0.2N aqueous HCl (200 mL) was added and the reaction mixture was stirred for 5 min. The organic layer was separated and washed with 0.2N aqueous HCl (1×200 mL), saturated aqueous NaHCO3 (2×200 mL) and brine (1×200 mL). The combined organic layers were dried with sodium sulfate, filtered and the solvent was removed under reduced pressure. The residue was dried under high vacuo overnight to yield the title compound as white foam (62.6 g) which was used without further purification. UPLC-MS: MS 459.3/461.3 (M+H+); UPLC rt 1.13 min.
후처리
- stirringthe reaction mixture was stirred for 5 min
- customThe organic layer was separated
- washwashed with 0.2N aqueous HCl (1×200 mL), saturated aqueous NaHCO3 (2×200 mL) and brine (1×200 mL)
- dry with materialThe combined organic layers were dried with sodium sulfate
- filtrationfiltered
- customthe solvent was removed under reduced pressure
- customThe residue was dried under high vacuo overnight
출처 및 근거
- ORD 기록
- ord-cc6a87f54fe644618d19194b6a5d38d5
- 출처 데이터셋
- uspto-grants-2014_10
- 특허 번호
- US08853203B2
반응 노트
불러오는 중…