تفاعل #657320

ord-32df2614b91f4eb19b253315662d9639

معادلة التفاعل

[NH4+].[OH-]
NH4OH
O
water
Nc1[nH]nc(-c2ccccc2)c1Br
4-bromo-3-phenyl-1H-pyrazole-5-amine
COC(CC(OC)OC)OC
1,1,3,3-tetramethoxypropane
Brc1c(-c2ccccc2)nn2cccnc12
3-bromo-2-phenylpyrazolo[1,5-a]pyrimidine
المردود 76.6%

المذيبات

ظروف التفاعل

درجة الحرارة
110°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with dichloromethane (3×100 mL)
  2. 2
    تجفيفThe organic layer is dried over anhydrous magnesium sulphate
  3. 3
    ترشيحfiltered
  4. 4
    تركيزconcentrated under reduced pressure
  5. 5
    أخرىThe crude material is purified by column chromatography

الإجراء التجريبي

To a solution of 4-bromo-3-phenyl-1H-pyrazole-5-amine (5.0 g, 0.02 mol) in acetic acid (50 mL) is added 1,1,3,3-tetramethoxypropane (4.14 g, 0.025 mol). The mixture is stirred at 110° C. for 1 h. The reaction mixture is then poured into water, basified with NH4OH and extracted with dichloromethane (3×100 mL). The organic layer is dried over anhydrous magnesium sulphate, filtered and concentrated under reduced pressure. The crude material is purified by column chromatography using silica gel in dichloromethane and ethyl acetate (1:0 to 95:5) as eluent and 4.2 g (75%) of 3-bromo-2-phenylpyrazolo[1,5-a]pyrimidine are obtained as a beige solid.

المصدر

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