반응식
CO[C:3](=O)[CH2:4][CH2:5][C:6]1[CH:11]=[C:10]([CH3:12])[C:9]([C:13]2NC3C=C(C4OC(NC5C=CC(OC)=CC=5)=NN=4)C=CC=3N=2)=[C:8]([CH3:36])[CH:7]=1.N([O-])=O.[Na+].C[OH:43].C([P:47](=[O:54])([O:51][CH2:52][CH3:53])[O:48][CH2:49][CH3:50])C=C>[H+].[B-](F)(F)(F)F.O.CC([O-])=O.CC([O-])=O.[Pd+2]>[CH2:49]([O:48][P:47]([CH2:3]/[CH:4]=[CH:5]/[C:6]1[CH:7]=[C:8]([CH3:36])[C:9]([CH:13]=[O:43])=[C:10]([CH3:12])[CH:11]=1)(=[O:54])[O:51][CH2:52][CH3:53])[CH3:50]참가 물질
반응물 4
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- 0 °C
실험 절차
To a suspension of 4-amino-2,6-dimethylbenzaldehyde (3.0 g, 20.1 mmol) (Example 1-60, step B) in enough 42% HBF4 to be stirred at 0° C. was added a solution of NaNO2 (1.39 g, 20.1 mmol) in water (10 ml) slowly. After 30 min at 0° C., MeOH (50 mL) was added and followed by Pd(OAc)2 (677 mg) and diethyl allylphosphonate (5.38 g, 30.2 mmol). The reaction mixture was heated at 80° C. for 30 min and the suspension was filtered through Celite, washed with CH2Cl2. The filtrate was extracted with CH2Cl2 and the combined organic layers were washed with water, brine, dried with MgSO4, and filtered. The solvent was removed under reduced pressure and the residue was purified by flash chromatography using a gradient of heptane/EtOAc (10:1 to 5:1 then followed by 100% EtOAc) to give the title compound as a light yellow oil. MS: m/z 311 (M+1).
후처리
- temperatureThe reaction mixture was heated at 80° C. for 30 min
- filtrationthe suspension was filtered through Celite
- washwashed with CH2Cl2
- extractionThe filtrate was extracted with CH2Cl2
- washthe combined organic layers were washed with water, brine
- dry with materialdried with MgSO4
- filtrationfiltered
- customThe solvent was removed under reduced pressure
- customthe residue was purified by flash chromatography
출처 및 근거
- ORD 기록
- ord-66bd870ee3284d83b6b1ff5d37893e27
- 출처 데이터셋
- uspto-grants-2011_02
- 특허 번호
- US07879850B2
연결된 노트
불러오는 중…