Triethylamine → 2-Bromo-4-(prop-1-ynyl)pyridine
反応式
[Br:1][C:2]1[CH:7]=[C:6](I)[CH:5]=[CH:4][N:3]=1.C[Si](C)(C)[C:11]#[C:12][CH3:13].C(N(CC)CC)C.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>C1(C)C=CC=CC=1.[Cu]I.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[Br:1][C:2]1[CH:7]=[C:6]([C:11]#[C:12][CH3:13])[CH:5]=[CH:4][N:3]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 3
実験手順
To a solution of 2-bromo-4-iodopyridine (2 g, 7.04 mmol), copper(I) iodide (0.080 mL, 2.11 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.407 g, 0.35 mmol) in toluene (85 mL) was added 1-(trimethylsilyl)-1-propyne (1.054 mL, 7.04 mmol), triethylamine (3.24 mL, 23.25 mmol) and tetrabutylammonium fluoride (1 M in THF, 7.04 mL, 7.04 mmol) and the resulting mixture was stirred under an argon atmosphere at r.t. overnight. The mixture was concentrated and the resulting residue was partitioned between water (10 mL) and DCM (10 mL) and poured into a phase separator. The organic phase was collected, and the aqueous phase was extracted once with DCM (10 mL). The combined organics were concentrated and purified by flash chromatography using 0% to 30% EtOAc in heptane to give the title compound (1.195 g, 87% yield): 1H NMR (500 MHz, DMSO-d6) δ ppm 2.11 (s, 3H), 7.42 (dd, 1H), 7.65 (s, 1H), 8.35 (dd, 1H); MS (ES+) m/z 196 [M+H]+; MS (APCI+) m/z 196 [M+H]
後処理
- concentrationThe mixture was concentrated
- customthe resulting residue was partitioned between water (10 mL) and DCM (10 mL)
- additionpoured into a phase separator
- customThe organic phase was collected
- extractionthe aqueous phase was extracted once with DCM (10 mL)
- concentrationThe combined organics were concentrated
- custompurified by flash chromatography
出典と根拠
- ORDレコード
- ord-efefc92146d948a39f7c9022bc0045c7
- 出典データセット
- uspto-grants-2016_02
- 特許番号
- US09248129B2
反応ノート
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