Cesium carbonate → HCID 86686004, 화합물
반응식
Br[C:2]1[CH:3]=[C:4](NC)[CH:5]=[N:6][CH:7]=1.[Cl:10][C:11]1[CH:12]=[C:13]2[C:17](=[CH:18][CH:19]=1)[C:16](=[O:20])[NH:15][C:14]2([CH3:22])[CH3:21].C([O-])([O-])=O.[Cs+].[Cs+].[NH2:29][C@H:30]1CCCC[C@@H]1N>O1CCOCC1.[Cu]I.O>[NH2:29][CH2:30][C:4]1[CH:3]=[C:2]([N:15]2[C:14]([CH3:22])([CH3:21])[C:13]3[C:17](=[CH:18][CH:19]=[C:11]([Cl:10])[CH:12]=3)[C:16]2=[O:20])[CH:7]=[N:6][CH:5]=1참가 물질
8
반응물 4
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- 150 °C
실험 절차
In a 25 mL sealed tube, a mixture of (5-bromo-pyridin-3-yl)-methylamine (281 mg, 1.5 mmol), 5-chloro-3,3-dimethyl-2,3-dihydro-isoindol-1-one (intermediate A-12, 196 mg, 1.0 mmol), CuI (38 mg, 0.2 mmol), Cs2CO3 (652 mg, 2.0 mmol) and (+)—(S,S)—1,2-diaminocyclohexane (68.4 mL, 0.6 mmol) were dissolved in dioxane (3 mL). The resulting reaction mixture was heated at 150° C. for 7 hours before it was poured into water (10 mL) and extracted with EtOAc (20 mL×2). The combined organic layers were washed with brine, dried over anhy. Na2SO4, filtered and concentrated in vacuo to give a crude product (320 mg, 100%). Without further purification, it was used directly in the next step. MS: 302.1 (M+H+).
후처리
- customIn a 25 mL sealed tube
- customThe resulting reaction mixture
- extractionextracted with EtOAc (20 mL×2)
- washThe combined organic layers were washed with brine
- customdried over anhy
- filtrationNa2SO4, filtered
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-a045474e7d3647c88ce68d355953461a
- 출처 데이터셋
- uspto-grants-2015_09
- 특허 번호
- US09133158B2
반응 노트
불러오는 중…