2-(Dimethylamino)ethanol → 2-(2-Dimethylaminoethoxy)-5-nitropyridine

HRID 1512101노트

반응식

HRID 1512101 반응식
[H-].[Na+].Cl[C:4]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[CH:6][N:5]=1.[CH3:13][N:14]([CH3:18])[CH2:15][CH2:16][OH:17]>O1CCCC1>[N+:10]([C:7]1[CH:8]=[CH:9][C:4]([O:17][CH2:16][CH2:15][N:14]([CH3:18])[CH3:13])=[N:5][CH:6]=1)([O-:12])=[O:11]

참가 물질

5

반응물 3

HCID 79022-(Dimethylamino)ethanolHCID 24758Sodium hydride2회HCID 783082-Chloro-5-nitropyridine

생성물 1

HCID 529049082-(2-Dimethylaminoethoxy)-5-nitropyridine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

Sodium hydride and oil bath heating. To a mixture of sodium hydride (189 mg, 4.73 mmol) in anhydrous tetrahydrofuran (2 mL) at 0° C. a solution of 2-chloro-5-nitropyridine (500 mg, 3.16 mmol) and 2-(dimethylamino)ethanol (353 mg, 3.96 mmol) in anhydrous tetrahydrofuran (4 mL) was added dropwise. The reaction was warmed to room temperature and stirred for 16 h. The THF was evaporated, and water (100 mL) and EtOAc (200 mL) were added. The aqueous layer was extracted with EtOAc (200 mL), and the organic layers combined, washed with brine, dried over sodium sulfate and concentrated to give a brown oil. Purification column chromatography on silica gel using 5% methanol/methylene chloride yielded 2-(5-nitropyridin-2-yloxy)-N,N-dimethylethanamine as a light yellow solid (233=mg, 35%). LC/MS (m/z): 212.2 (MH+), Rt 1.28 minutes.

후처리

  1. additionwas added dropwise
  2. customThe THF was evaporated
  3. additionwater (100 mL) and EtOAc (200 mL) were added
  4. extractionThe aqueous layer was extracted with EtOAc (200 mL)
  5. washwashed with brine
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated
  8. customto give a brown oil
  9. customPurification column chromatography on silica gel using 5% methanol/methylene chloride

출처 및 근거

ORD 기록
ord-10f00b88449444f3a3776427f64defb7
출처 데이터셋
uspto-grants-2012_07
특허 번호
US08217035B2

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