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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446284Generated: October 27, 2026

Diisopropylethylamine → 2-{(3R)-1-[(3-pyridin-2-ylisoxazol-4-yl)carbonyl]piperidin-3-yl}propan-2-ol

https://huagongshe.com/reaction/1446284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant5-(Pyridin-2-yl)-1,2-oxazole-4-carboxylic acidHCID 22309070—
Reactant(R)-2-(piperidin-3-yl)propan-2-ol hydrochlorideHCID 68537144—
SolventDimethylformamideHCID 6228—
Product2-{(3R)-1-[(3-pyridin-2-ylisoxazol-4-yl)carbonyl]piperidin-3-yl}propan-2-olHCID 6868502148.8%

Reaction Steps

A solution of 2-[(3R)-piperidin-3-yl]propan-2-ol hydrochloride (7 mg, 0.039 mmol), TBTU (15 mg, 0.047 mmol, 1.2 equ.) and N-ethyl-N-isopropylpropan-2-amine (14 μL, 0.079 mmol, 2 equ.) in DMF (0.3 mL) was added to 5-pyridin-2-ylisoxazole-4-carboxylic acid (7 mg, 0.039 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 (6 mg). MS (ESI, pos. ion) m/z calcd for C17H21N3O3: 315.1583, found 315.1586.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666888B2
Source datasetuspto-grants-2010_02
ORD IDord-6515d54e4e12421e856c87cbb832b7f9
Source noteuspto-grants-2010_02