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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 659230Erstellt: 25. Oktober 2026

Diisopropylethylamine → HCID 58062981, Verbindung

https://huagongshe.com/reaction/659230

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt2-Methoxy-4,6-bis(trifluoromethyl)benzoic acidHCID 2741287—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Eduktcis-2-Pyrrolidin-1-yl-cyclohexylamine dihydrochlorideHCID 66680564—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 58062981HCID 5806298152,2%

Reaktionsschritte

2,4-Bis(trifluoromethyl)-6-methoxy-benzoic acid (200 mg, 0.69 mmol) was dissolved in 5 mL dimethylformamide. N,N-Diisopropyl ethyl amine (359 mg, 2.8 mmol) and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (264 mg, 0.69 mmol) were added. After 5 minutes of stirring at room temperature cis-2-pyrrolidin-1-yl-cyclohexylamine dihydrochloride (intermediate F) (171 mg, 0.71 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 (dichloromethane/methanol/ammonia 100:0:0→140:10:1) yielded cis-2-methoxy-N-(2-pyrrolidin-1-yl-cyclohexyl)-4,6-bis-trifluoromethyl-benzamide as a white solid (158 mg, 52%), MS: m/e=439.2 [(M+H)+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08080541B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-eb70b7417188446885fccc12434d259f
Quellennotizuspto-grants-2011_12