تفاعل #358881

ord-5b94af4bbe6c4657a23fd451866e8a47

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةrefluxed for a further 5 h
  2. 2
    درجة الحرارةAfter the solution has cooled the insoluble salts
  3. 3
    ترشيحare filtered off
  4. 4
    تجفيفThe organic phase is dried over MgSO4
  5. 5
    workup.ADDITIONA 4:1 mixture of 5-nitro-1-(2-pyrrolidin-1-yl-ethyl)-1H-indazole

الإجراء التجريبي

10.5 g (62.0 mmol) 1-(2-chloroethyl)-pyrrolidine hydrochloride and 12.9 g (93.0 mmol) K2CO3 are added successively to a solution of 5.00 g (31.0 mmol) 5-nitroindazole in 100 mL acetonitrile. The reaction solution is stirred for 2 h at RT and refluxed for a further 5 h. After the solution has cooled the insoluble salts are filtered off and the solvent is eliminated i.vac. The residue is taken up in EtOAc and water. The organic phase is dried over MgSO4 and the solvent is eliminated i.vac. A 4:1 mixture of 5-nitro-1-(2-pyrrolidin-1-yl-ethyl)-1H-indazole and 5-nitro-2-(2-pyrrolidin-1-yl-ethyl)-2H-indazole is obtained. The purification is carried out by column chromatography on Alox (PE/EtOAc 3:2).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07452911B2uspto-grants-2008_11