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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39437Erstellt: 24. Oktober 2026

Diisopropylethylamine → 2-Cyclopropyl-N-((3SR,4RS)-4-pyrrolidin-1-yl-tetrahydro-pyran-3-yl)-4-trifluoromethyl-benzamide

https://huagongshe.com/de/reaction/39437

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Edukt2-Cyclopropyl-4-(trifluoromethyl)benzoic acidHCID 59438485—
Edukt4-(Pyrrolidin-1-yl)tetrahydro-2H-pyran-3-amine dihydrochlorideHCID 67360004—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-Cyclopropyl-N-((3SR,4RS)-4-pyrrolidin-1-yl-tetrahydro-pyran-3-yl)-4-trifluoromethyl-benzamideHCID 6735925562%

Reaktionsschritte

2-Cyclopropyl-4-trifluoromethyl-benzoic acid (intermediate J, 118 mg, 0.513 mmol) was dissolved in 2.5 mL dimethylformamide. N,N-Diisopropyl ethyl amine (338 mg, 2.62 mmol) and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (195 mg, 0.513 mmol) were added. After 10 minutes of stirring at room temperature trans-(4-pyrrolidin-1-yl-tetrahydro-pyran-3-ylamine dihydrochloride (intermediate 1,187 mg, 0.769 mmol) was added. The reaction mixture was stirred at room temperature overnight. The solvent was evaporated off. The residue was taken up in 2N sodium carbonate solution and ethyl acetate and was extracted three times with ethyl acetate. The combined organic phases were dried on sodium sulfate, filtered and evaporated. Purification of the residue by flash chromatography on silica gel (heptane/ethyl acetate/triethylamine 1:0:0→10:10:1) yielded the title compound as a white solid (121 mg, 62%), MS: m/e=383.3 [(M+H)+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524909B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-fac9c8face704ca2b24997f1ae65abf9
Quellennotizuspto-grants-2013_09