Hydrochloric Acid → 4-(5-Aminopyridin-2-yl)-1-(2-hydroxy-2-methylpropyl)piperidine-4-carbonitrile

HRID 1748519노트

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HRID 1748519 반응식
C(=[NH:14])(C1C=CC=CC=1)C1C=CC=CC=1.Br[C:16]1[CH:17]=[CH:18][C:19]([C:22]2([C:33]#[N:34])[CH2:27][CH2:26][N:25]([CH2:28][C:29]([OH:32])([CH3:31])[CH3:30])[CH2:24][CH2:23]2)=[N:20][CH:21]=1.C(P(C(C)(C)C)C1C=CC2C(=CC=CC=2)C=1C1C2C(=CC=CC=2)C=CC=1)(C)(C)C.CC(C)([O-])C.[Na+].Cl.C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1.C([O-])(=O)C.[Pd+2].C([O-])(=O)C.O>[NH2:14][C:16]1[CH:17]=[CH:18][C:19]([C:22]2([C:33]#[N:34])[CH2:27][CH2:26][N:25]([CH2:28][C:29]([OH:32])([CH3:31])[CH3:30])[CH2:24][CH2:23]2)=[N:20][CH:21]=1

참가 물질

10

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온도
120 °C

실험 절차

Benzophenonimine (2.22 g) was added to a suspension of 4-(5-bromopyridin-2-yl)-1-(2-hydroxy-2-methylpropyl)piperidine-4-carbonitrile (3.95 g), palladium (II) acetate (328 mg), racemic-2-(di-tert-butylphosphino)-1,1′-binaphthyl (909 mg) and sodium tert-butoxide (1.68 g) in toluene (29 ml), and stirred at 120° C. for 2.5 hours. The reaction solution was left stand, a mixture of concentrated hydrochloric acid (2 ml) and water (6 ml) were added at 60-80° C. and stirred at room temperature. A saturated aqueous solution of sodium bicarbonate was added to the reaction solution and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified with basic silica gel column chromatography (n-hexane/ethyl acetate) to give the titled compound (2.6 g) as a pale yellow solid.

후처리

  1. waitThe reaction solution was left stand
  2. additionwere added at 60-80° C.
  3. stirringstirred at room temperature
  4. extractionextracted with ethyl acetate
  5. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified with basic silica gel column chromatography (n-hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-407f97cfb8a643a19128679650219744
출처 데이터셋
uspto-grants-2015_10
특허 번호
US09150555B2

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