تفاعل #1833285

ord-05913cbe04fc45659213b15cce14fd5a

معادلة التفاعل

O=[N+]([O-])c1cnn(Cc2cc(Cl)ccc2OCc2ccccc2)c1
1-({5-chloro-2-[(phenylmethyl)oxy]phenyl}methyl)-4-nitro-1H-pyrazole
Nc1cnn(Cc2cc(Cl)ccc2OCc2ccccc2)c1
title compound
Nc1cnn(Cc2cc(Cl)ccc2OCc2ccccc2)c1
1-({5-Chloro-2-[(phenylmethyl)oxy]phenyl}methyl)-1H-pyrazol-4-amine

المذيبات

ظروف التفاعل

درجة الحرارة
85°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلThe reaction mixture was applied to a 20 g SCX-2 cartridge (pre-washed with MeOH)
  2. 2
    غسيلthe cartridge washed with methanol (6 column volumes)
  3. 3
    غسيلThe product was eluted with 10% NH3 (aqueous) in MeOH (4 column volumes)
  4. 4
    تركيزThe combined basic fractions were concentrated in vacuo
  5. 5
    أخرىpurified on silica (50 g)
  6. 6
    أخرىevaporated in vacuo

الإجراء التجريبي

To a solution of 1-({5-chloro-2-[(phenylmethyl)oxy]phenyl}methyl)-4-nitro-1H-pyrazole (for a preparation see intermediate 8; 476 mg, 1.39 mmol) in ethanol (15 ml) was added stannous chloride (hydrated) (1.59 g, 7.03 mmol) and the reaction stirred at 85° C. overnight, under nitrogen. The reaction mixture was applied to a 20 g SCX-2 cartridge (pre-washed with MeOH) and the cartridge washed with methanol (6 column volumes). The product was eluted with 10% NH3 (aqueous) in MeOH (4 column volumes). The combined basic fractions were concentrated in vacuo. The residue was loaded in dichloromethane and purified on silica (50 g) using 0-100% ethyl acetate-cyclohexane. The appropriate fractions were combined and evaporated in vacuo to give the title compound (191 mg) as a red gum; LCMS (System 1): MH+=314, tRET=2.69 min.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09149462B2uspto-grants-2015_10