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Potassium Carbonate → cis-4-(6-Bromo-2-pyridinyl)-2,6-dimethylmorpholine

HRID 2278424
ノート
印刷プレビュー

反応式

HRID 2278424 の反応式
[CH3:1][C@H:2]1[O:7][C@@H:6]([CH3:8])[CH2:5][NH:4][CH2:3]1.[Br:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12](Br)[N:11]=1.C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[Br:9][C:10]1[N:11]=[C:12]([N:4]2[CH2:5][C@H:6]([CH3:8])[O:7][C@H:2]([CH3:1])[CH2:3]2)[CH:13]=[CH:14][CH:15]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 11430Potassium CarbonateHCID 122742,6-DibromopyridineHCID 6415002,6-Dimethylmorpholine, cis-

生成物 1

HCID 86702423cis-4-(6-Bromo-2-pyridinyl)-2,6-dimethylmorpholine

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

反応条件

温度
120 °C

実験手順

cis-2,6-Dimethylmorpholine (0.535 g, 4.64 mmol) was added to a suspension of 2,6-dibromopyridine (1 g, 4.22 mmol) and potassium carbonate (1.750 g, 12.66 mmol) in anhydrous acetonitrile (35 mL). After addition, the reaction mixture was stirred at 120° C. overnight. Crude LC/MS showed starting material and desired product so cis-2,6-dimethylmorpholine (185 mg, 1.61 mmol) was added to the reaction mixture which was then stirred at 120° C. overnight. Crude LC/MS showed desired product can be seen and no starting material left, so the reaction mixture was diluted with ethyl acetate (100 mL) and water (50 mL). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (2×100 mL). The combined organic layers were dried (sodium sulfate), filtered and concentrated under reduced pressure. The residue was dissolved in dichloromethane (˜10 ml) and purified on silica by a Biotage SP4 chromatographic system (40+M cartridge, eluted with 0-100% ethyl acetate in isohexanes). Fractions containing pure product were combined and concentrated under reduced pressure to give the title compound as a colourless oil (705 mg, 2.340 mmol, 55.4% yield). LC/MS [M+H]+=271/273.

後処理

  1. additionAfter addition

出典と根拠

ORDレコード
ord-2b999aa314e64ce48cf06e1e0afcadd0
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09133178B2

反応ノート

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