تفاعل #159367

ord-81c88674567548589f2b42bc6eb3856d

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction mixture was evacuated with vacuum
  2. 2
    أخرىpurged with H2 (3×)
  3. 3
    ترشيحThe reaction mixture was then filtered through a pad of Celite®
  4. 4
    تركيزThe filtrate was concentrated in vacuo
  5. 5
    أخرىthe crude was purified by column chromotagraphy (Si-PPC, gradient 0 to 30% methanol in dichloromethane)

الإجراء التجريبي

To a solution of 1,3-dimethyl-4-nitro-1H-pyrazole-5-carboxamide (730 mg, 3.96 mmol) in anhydrous ethanol (100 mL) and ethyl acetate (100 mL) was added 10 wt % Pd on carbon (100.0 mg). The reaction mixture was evacuated with vacuum and purged with H2 (3×), then stirred under H2 at 50 psi for 5 hours. The reaction mixture was then filtered through a pad of Celite®. The filtrate was concentrated in vacuo and the crude was purified by column chromotagraphy (Si-PPC, gradient 0 to 30% methanol in dichloromethane) to get the desired product (597.0 mg, 97.7%) as a solid. 1H NMR (DMSO-d6, 400 MHz) δ ppm 7.26 (br s, 2H), 4.03 (br s, 2H), 3.84 (s, 3H), 2.02 (s, 3H); LC-MS m/z (method A)=155.2 [M+H]+, RT=0.35 min.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08828990B2uspto-grants-2014_09