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Hydrochloric Acid → 2'-Methyl-2-oxo-1,2-dihydro-3,4'-bipyridine-6-carboxylic acid, hydrochloride salt

HRID 2364968
ノート
印刷プレビュー

反応式

HRID 2364968 の反応式
Br[C:2]1[CH:3]=[CH:4][C:5]([C:10]([O:12]C)=[O:11])=[N:6][C:7]=1[O:8]C.Br[C:15]1[CH:16]=[CH:17][C:18]([C:23](=N)OC)=[N:19][C:20]=1OC.[ClH:27]>CO>[ClH:27].[CH3:23][C:18]1[CH:17]=[C:16]([C:2]2[C:7](=[O:8])[NH:6][C:5]([C:10]([OH:12])=[O:11])=[CH:4][CH:3]=2)[CH:15]=[CH:20][N:19]=1
参加物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 313Hydrochloric AcidHCID 46311222Methyl 5-bromo-6-methoxypicolinateHCID 68380252Methyl 5-bromo-6-methoxypyridine-2-carboximidoate

生成物 1

HCID 1317313152'-Methyl-2-oxo-1,2-dihydro-3,4'-bipyridine-6-carboxylic acid, hydrochloride salt

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Synthesis of methyl 5-bromo-6-methoxypyridine-2-carboxylate (C30). A stirred solution of methyl 5-bromo-6-methoxypyridine-2-carboximidoate (C29) (9.42 g, 38.4 mmol) in methanol (66 mL) and concentrated hydrochloric acid (6.6 mL) was heated under reflux for 18 hours. The reaction was concentrated to dryness under reduced pressure. The resulting solid was dissolved in dichloromethane (500 mL) and washed with saturated aqueous sodium bicarbonate solution (250 mL). The aqueous phase was extracted with dichloromethane (200 mL), and the combined organics were washed with water (250 mL), with saturated aqueous sodium chloride solution (250 mL), dried over magnesium sulfate and concentrated under reduced pressure to provide the title compound. The reaction was repeated on additional material (1.65 g, 6.73 mmol), worked up in a similar manner, combined with the first reaction, and purified by silica gel chromatography (Eluant: 10% ethyl acetate in heptane) to provide the title compound as a yellow solid. Yield: 4.48 g, 18.2 mmol, 40%. LCMS m/z 246.1 (M+1). 1H NMR (400 MHz, CDCl3) δ 3.97 (s, 3H), 4.11 (s, 3H), 7.59 (d, J=7.8 Hz, 1H), 7.93 (d, J=7.8 Hz, 1H).

後処理

  1. temperatureunder reflux for 18 hours
  2. concentrationThe reaction was concentrated to dryness under reduced pressure
  3. dissolutionThe resulting solid was dissolved in dichloromethane (500 mL)
  4. washwashed with saturated aqueous sodium bicarbonate solution (250 mL)
  5. extractionThe aqueous phase was extracted with dichloromethane (200 mL)
  6. washthe combined organics were washed with water (250 mL), with saturated aqueous sodium chloride solution (250 mL)
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-d8bef0c1209947b2aabb14ddae4fd322
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08697673B2

反応ノート

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