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HRID 1446299Erstellt: 26. Oktober 2026

Diisopropylethylamine → 3-({1-[(3-Methyl-5-phenylisoxazol-4-yl)carbonyl]pyrrolidin-2-yl}methyl)pyridine

https://huagongshe.com/reaction/1446299

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Edukt3-Methyl-5-phenylisoxazole-4-carboxylic acidHCID 2776514—
Edukt3-(2-Pyrrolidinylmethyl)pyridineHCID 3263876—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-({1-[(3-Methyl-5-phenylisoxazol-4-yl)carbonyl]pyrrolidin-2-yl}methyl)pyridineHCID 59170244—

Reaktionsschritte

3-Methyl-5-phenyl-4-isoxazolecarboxylic acid (40 mg, 0.197 mmol), 3-(pyrrolidin-2-ylmethyl)pyridine (50.5 mg, 0.215 mmol), O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (86.2 mg, 0.268 mmol) and diisopropylethylamine (25.4 mg, 0.197 mmol) were mixed in dimethylformamide (1.0 mL) and stirred at room temperature. Solvent was evaporated in vacuo, and the residue was taken up in methanol (1 mL), filtered and purified by preparative chromatography. The combined fractions were partitioned between NaHCO3 (sat) and ethylacetate. The organic layer was washed with water and concentrated in vacuo to afford the title compound. HRMS (ESI, pos. ion) m/z calcd for C21H21N3O2: 347.1634, found 347.1642.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07666888B2
Quelldatensatzuspto-grants-2010_02
ORD IDord-95b6aeec88fd4f12ad0a50e3f22fc281
Quellennotizuspto-grants-2010_02