Water → HCID 67608342, 화합물

HRID 925288노트

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HRID 925288 반응식
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([C:9]#[N:10])[N:6]=[C:5]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][N:12]=2)[CH:4]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3].O.[OH-].[Na+]>O1CCCC1>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([CH2:9][NH2:10])[N:6]=[C:5]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][N:12]=2)[CH:4]=1

참가 물질

6

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온도
25 °C

실험 절차

Over a solution of 4-Methoxy-[2,2′]bipyridinyl-6-carbonitrile (5.0 g, 23.7 mmol) in tetrahydrofuran (25 mL), a 1.0 M solution of LiAlH4 in tetrahydrofuran (75 mL, 75.0 mmol) was slowly added and the reaction mixture was stirred for 2 h at 25° C. The reaction was then cooled to 0° C., water (2.5 mL) followed by a 15% aqueous solution of NaOH (2.5 mL) were slowly added and stirred at 25° C. for 16 hours. The reaction mixture was filtered through celite, washed with tetrahydrofuran and the organic solvent removed under reduced pressure. The aqueous residue was extracted with dichloromethane, the organic solvent dried with sodium sulphate anhydrous, filtered and removed under reduced pressure to afford C-(4-Methoxy-[2,2′]bipyridinyl-6-yl)-methylamine as an orange oil (3.5 g, aprox 68%) that was used in the next step without purification.

후처리

  1. temperatureThe reaction was then cooled to 0° C.
  2. additionwere slowly added
  3. stirringstirred at 25° C. for 16 hours
  4. filtrationThe reaction mixture was filtered through celite
  5. washwashed with tetrahydrofuran
  6. customthe organic solvent removed under reduced pressure
  7. extractionThe aqueous residue was extracted with dichloromethane
  8. dry with materialthe organic solvent dried with sodium sulphate anhydrous
  9. filtrationfiltered
  10. customremoved under reduced pressure

출처 및 근거

ORD 기록
ord-8a1f380a632a42ebb0ed3d57bdce8740
출처 데이터셋
uspto-grants-2016_03
특허 번호
US09284296B2

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