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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446287Generated: October 26, 2026

Diisopropylethylamine → {(4R)-4-phenyl-1-[(5-pyridin-2-ylisoxazol-4-yl)carbonyl]pyrrolidin-3-yl}methanol

https://huagongshe.com/reaction/1446287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant(4-Phenylpyrrolidin-3-yl)methanolHCID 13316928—
Reactant5-(Pyridin-2-yl)-1,2-oxazole-4-carboxylic acidHCID 22309070—
SolventDimethylformamideHCID 6228—
Product{(4R)-4-phenyl-1-[(5-pyridin-2-ylisoxazol-4-yl)carbonyl]pyrrolidin-3-yl}methanolHCID 6868304726%

Reaction Steps

A solution of (4-phenylpyrrolidin-3-yl)methanol (7 mg, 0.033 mmol), TBTU (13 mg, 0.039 mmol, 1.2 equ.) and N-ethyl-N-isopropylpropan-2-amine (11 μL, 0.066 mmol, 2 equ.) in DMF (0.3 mL) was added to 5-pyridin-2-ylisoxazole-4-carboxylic acid (6 mg, 0.033 mmol) and the reaction mixture was stirred at rt for 2 h. The solvent was evaporated and the crude product was purified by RP-HPLC. After evaporation of the solvents from the pure fractions, the residue was dissolved in chloroform and washed with diluted NaOH to provide the neutral compound in the organic phase that was dried (Na2SO4) and evaporated and dried in vacuum to yield the title compound (3 mg). MS (ESI, pos. ion) m/z calcd for C20H19N3O3: 349.1426, found 349.1427.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666888B2
Source datasetuspto-grants-2010_02
ORD IDord-455bdb12276c450c81f770d057345e5c
Source noteuspto-grants-2010_02