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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77582Erstellt: 25. Oktober 2026

Trifluoroacetic acid → HCID 86762769, Verbindung

https://huagongshe.com/reaction/77582

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktDiisopropylethylamineHCID 81531—
Edukt2-Chloro-5-fluoropyrimidineHCID 583466—
EduktHCID 86762770HCID 86762770—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelSodium CarbonateHCID 10340—
ProduktHCID 86762769HCID 8676276941%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A solution of N-[3-[(4aR,7aS)-2-benzamido-4a,5,6,7-tetrahydro-4H-pyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-fluoro-pyridine-2-carboxamide; 2,2,2-trifluoroacetic acid (150 mg, 254 μmol), 5-fluoro-2-chloropyrimidine (68 mg, 51 μmol) and diisopropylethylamine (98 μL, 56 μmol) is heated in dimethyl sulfoxide (5 mL) overnight at 40° C. Additional 5-fluoro-2-chloropyrimidine (68 mg, 51 μmol) and diisopropylethylamine (98 μL, 56 μmol) is added and the mixture is heated overnight at 50° C. Additional 5-fluoro-2-chloropyrimidine (68 mg, 51 μmol) and diisopropylethylamine (98 μL, 56 μmol) is added and the mixture is heated overnight at 50° C. for a third night. The reaction is cooled, diluted with saturated aqueous sodium carbonate (50 mL) to give a slurry that is filtered and dried in a vacuum oven at 50° C. for 4 hours to give the title compound (60 mg, 41%). ES/MS (m/e): 449 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841293B1
Quelldatensatzuspto-grants-2014_09
ORD IDord-a8ead401e87b41a0ab024ab02b50ac0d
Quellennotizuspto-grants-2014_09