Réaction #10388

Équation de réaction

4-[3-(tert-Butoxycarbonylamino)-pyrrolidin-1-yl]-2,5-difluorobenzoic acid ethyl ester

isopropylamine

→

title compound

Rendement 28.1%

4-[3-(tert-Butoxycarbonylamino)pyrrolidin-1-yl]-5-fluoro-2-isopropylaminobenzoic acid ethyl ester

Rendement 28.1%

Solvants

dimethyl sulfoxide

Conditions de réaction

Traitement

1. 1
   AutreThe excess amine is removed
2. 2
   FiltrationThe residue is filtered
3. 3
   Concentrationconcentrated under vacuum to a thick oil
4. 4
   AutrePurification by column chromatography (1:1:7 ethyl acetate/chloroform/hexanes)

Mode opératoire

4-[3-(tert-Butoxycarbonylamino)-pyrrolidin-1-yl]-2,5-difluorobenzoic acid ethyl ester (Example 2j, 5.4 g, 13.9 mmol), isopropylamine (40 mL, 469 mmol), and dimethyl sulfoxide (25 mL) are heated at 100° C. for 4 days in a sealed glass tube. The excess amine is removed by blowing in compressed air. The residue is filtered and concentrated under vacuum to a thick oil. Purification by column chromatography (1:1:7 ethyl acetate/chloroform/hexanes) to provide the title compound as a solid (1.6 g). MS: m/z 410 (MH+).

Source