Réaction #657258

ord-94206c7107114397ac2b99f60be78715

Équation de réaction

CCOC(=O)c1cnn(C(c2ccccc2)(c2ccccc2)c2ccccc2)c1
ethyl-1-tritylpyrazole-4-carboxylate
COC(=O)c1cc(C(=O)OC)[nH]n1
dimethyl-3,5-pyrazoledicarboxylate
[H-].[Na+]
sodium hydride
ClC(c1ccccc1)(c1ccccc1)c1ccccc1
trityl chloride
COC(=O)c1cc(C(=O)OC)n(C(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Dimethyl 1-trityl-3,5-pyrazoledicarboxylate
Rendement 98.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrehas been isolated

Mode opératoire

This compound is a white microcrystalline solid that has been isolated following the methodology described in 2b for ethyl-1-tritylpyrazole-4-carboxylate, by reaction of with dimethyl-3,5-pyrazoledicarboxylate (1.411 g, 7.66 mmol) with sodium hydride (250 mg, 10.41 mmol) in dry dimethylformamide (20 mL), followed by treatment with trityl chloride (2.135 g, 7.66 mmol). Yield: 98% (3.200 g, 7.50 mmol).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09023315B2uspto-grants-2015_05