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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 43012Erstellt: 25. Oktober 2026

Potassium Carbonate → (S)-Ethyl 1-((2-(benzyloxycarbonylamino)-2,3-dihydro-1H-inden-5-yl)methyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/43012

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktThionyl ChlorideHCID 24386—
Edukt(S)-benzyl 5-(hydroxymethyl)-2,3-dihydro-1H-inden-2-ylcarbamateHCID 70224068—
EduktHCID 178469923HCID 178469923—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt(S)-Ethyl 1-((2-(benzyloxycarbonylamino)-2,3-dihydro-1H-inden-5-yl)methyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylateHCID 702445233,1%

Reaktionsschritte

(S)-Benzyl 5-(hydroxymethyl)-2,3-dihydro-1H-inden-2-ylcarbamate (2.96 mmol, 880 mg) was dissolved in DCM (10 mL) and thionyl chloride (5.92 mmol, 0.432 ml, 704 mg) added. The mixture was stirred at room temperature for 30 min TLC before the solvent was removed under reduced pressure and residual thionylchloride azeotroped with DCM (×3). To the residue was added potassium carbonate (8.88 mmol, 1227 mg) followed by DMF (8 ml) then ethyl 3-(trifluoromethyl)-1H-pyrazole-4-carboxylate (2.96 mmol, 616 mg) and the mixture heated to 60° C. After 1 h the mixture was concentrated and partitioned between EtOAc/H2O and the organic layer was washed with water (×3). The organic layer was dried, filtered and concentrated to give a yellow oil which was purified by flash chromatography eluting with 15% EtOAc/Heptane to give the desired isomer as a colourless oil (45 mg, 0.092 mmol, 3.1%). 1H NMR (400 MHz, CDCl3) δ 1.34 (t, 3H) 2.75 (m, 2H) 3.25 (m, 2H) 4.33 (q, 2H), 4.50 (m, 1H) 4.95 (m, 1H), 5.08 (s, 2H) 5.48 (s, 2H) 7.00 (m, 2H) 7.15 (d, 1H) 7.34 (m, 5H) 7.99 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536214B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-1f8ee166ea494577aee895538f08d7c0
Quellennotizuspto-grants-2013_09