反応 #657324

ord-edd0da8976ce407e9f845acbc83901a1

反応方程式

CC(=O)Nc1cc(-c2c(-c3ccc(F)cc3)nn3cccnc23)ccn1
N-{4-[2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl]pyridin-2-yl}acetamide
[BH4-].[Na+]
sodium borohydride
O
water
CC(=O)Nc1cc(-c2c(-c3ccc(F)cc3)nn3c2NCCC3)ccn1
N-{4-[2-(4-fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl]pyridin-2-yl}acetamide
収率 25.1%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The mixture is refluxed for 1 h
  2. 2
    抽出extracted with dichloromethane (3×20 mL)
  3. 3
    乾燥dried over anhydrous magnesium sulphate
  4. 4
    ろ過filtered
  5. 5
    濃縮concentrated under reduced pressure
  6. 6
    その他The crude material is purified by column chromatography

実験手順

To a mixture of N-{4-[2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl]pyridin-2-yl}acetamide (120 mg, 0.34 mmol, 1 eq) in 2 mL of ethanol is added sodium borohydride (29 mg, 0.76 mmol, 2.2 eq). The mixture is refluxed for 1 h. The mixture is then poured into water, extracted with dichloromethane (3×20 mL), dried over anhydrous magnesium sulphate, filtered and concentrated under reduced pressure. The crude material is purified by column chromatography using silica gel in heptane and ethyl acetate (1:0 to 0:1) as eluent and 30 mg (25%) of N-{4-[2-(4-fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl]pyridin-2-yl}acetamide are obtained as a white solid.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09023844B2uspto-grants-2015_05