Réaction #1998135

ord-644cffe4bd234ea8bea4b5433e1522c7

Solvants

Conditions de réaction

Température
105°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    ConcentrationThe reaction was concentrated in vacuo
  2. 2
    Autrethe resultant residue purified by flash chromatography (Biotage SP4, gradient 0-10% MeOH in EtOAc)

Mode opératoire

Ethyl 1-[2-(4-methoxyphenyl)-2-oxoethyl]-4-nitro-1H-pyrrole-2-carboxylate (610 mg, 1.8 mmol) was mixed with 1,4-dioxane (7 mL) and ethylene-1,2-diamine (1.7 mL) and the mixture heat at 105° C. After 24 hours the reaction was complete (monitored by LCMS). The reaction was concentrated in vacuo and the resultant residue purified by flash chromatography (Biotage SP4, gradient 0-10% MeOH in EtOAc) to give 10a-(4-methoxyphenyl)-7-nitro-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one (200 mg, yield 34%). ESI-MI m/z [M+H]+ 328.9.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08604034B2uspto-grants-2013_12