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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446298Generated: October 26, 2026

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

https://huagongshe.com/reaction/1446298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methyl-3-phenylisoxazole-4-carboxylic acidHCID 14343—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant3-(2-Pyrrolidinylmethyl)pyridineHCID 3263876—
SolventDimethylformamideHCID 6228—
Product3-({1-[(5-Methyl-3-phenylisoxazol-4-yl)carbonyl]pyrrolidin-2-yl}methyl)pyridineHCID 59170269—

Reaction Steps

5-Methyl-3-phenylisooxazole-4-carboxylic 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: 349.1426, found 349.1693.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666888B2
Source datasetuspto-grants-2010_02
ORD IDord-e787f621e2a44c7894952f4382656ff5
Source noteuspto-grants-2010_02