تفاعل #657329

ord-cbe0b4a2536f4ac0900ca83b08c5a10a

معادلة التفاعل

CC(=O)N(C(C)=O)c1cc(-c2c(-c3ccccc3)nn3cccnc23)ccn1
N-acetyl-N-[4-(2-phenylpyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-yl]acetamide
CCO
ethanol
[BH4-].[Na+]
sodium borohydride
O
water
CC(=O)N1CCCn2nc(-c3ccccc3)c(-c3ccnc(N(C(C)=O)C(C)=O)c3)c21
N-acetyl-N-[4-(4-acetyl-2-phenyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-yl]acetamide
المردود 46.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture is refluxed for 1 h
  2. 2
    استخلاصextracted with dichloromethane (3×50 mL)
  3. 3
    تجفيفdried over anhydrous magnesium sulphate
  4. 4
    ترشيحfiltered
  5. 5
    تركيزconcentrated under reduced pressure
  6. 6
    أخرىThe crude material is purified by column chromatography

الإجراء التجريبي

To a mixture of N-acetyl-N-[4-(2-phenylpyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-yl]acetamide (158 mg, 0.43 mmol, 1 eq) in 3 mL of ethanol is added sodium borohydride (35 mg, 0.94 mmol, 2.2 eq). The mixture is refluxed for 1 h. The mixture is then poured into water, extracted with dichloromethane (3×50 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 66 mg (46%) of N-acetyl-N-[4-(4-acetyl-2-phenyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-yl]acetamide are obtained as a white solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09023844B2uspto-grants-2015_05