Calcium Carbonate → HCID 90001797, 화합물
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Br[CH2:2][C:3]1[C:8]([I:9])=[CH:7][CH:6]=[C:5]([Cl:10])[N:4]=1.C([O-])([O-])=[O:12].[Ca+2]>O1CCOCC1.O>[Cl:10][C:5]1[N:4]=[C:3]([CH2:2][OH:12])[C:8]([I:9])=[CH:7][CH:6]=1.[Cl:10][C:5]1[N:4]=[C:3]([CH3:2])[C:8]([I:9])=[CH:7][CH:6]=1참가 물질
실험 절차
To a stirred solution of 2-bromomethyl-6-chloro-3-iodo-pyridine (20 g, crude, 60 mmol, 1 eq) in 1,4-dioxane (200 mL) was added suspension of CaCO3 (31.4 g, 313 mmol, 5.2 eq) in water (200 mL) at room temperature. Resulting reaction mixture was refluxed for 10 hours. After complete consumption of starting material, reaction mixture was cooled to room temperature and filtered through celite bed over Buchner funnel. Celite bed was washed with EtOAc (2×100 mL). Combined filtrate was washed with water (100 mL) and aqueous sodium bicarbonate (50 mL), dried over sodium sulfate and concentrated under reduced pressure to afford brown solid (21 g, crude). Crude was purified by column chromatography using silica gel (100-200 mesh). Desired compound was eluted at 20% EtOAc in hexane to get title compound as faint yellow solid (2.9 g, 18%) and also 9 g of 6-chloro-3-iodo-2-methyl-pyridine was recovered. 1H NMR (400 MHz, CDCl3) δ: 3.87 (t, J=4.9 Hz, 1H), 4.63 (d, J=4.96 Hz, 2H), 7.04 (d, J=4 Hz, 1H), 8.0 (d, J=8.2 Hz, 1H). LC-MS (m/z): 270.1 (M+H).
후처리
- customResulting
- customreaction mixture
- temperaturewas refluxed for 10 hours
- customAfter complete consumption of starting material, reaction mixture
- filtrationfiltered through celite bed over Buchner funnel
- washCelite bed was washed with EtOAc (2×100 mL)
- washCombined filtrate was washed with water (100 mL) and aqueous sodium bicarbonate (50 mL)
- dry with materialdried over sodium sulfate
- concentrationconcentrated under reduced pressure
- customto afford brown solid (21 g, crude)
- customCrude was purified by column chromatography
- washDesired compound was eluted at 20% EtOAc in hexane
출처 및 근거
- ORD 기록
- ord-2cf4188f39fa4eddba08c16a4218086a
- 출처 데이터셋
- uspto-grants-2015_09
- 특허 번호
- US09131697B2
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