HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 3-{1-[(5-Benzylisoxazol-4-yl)carbonyl]pyrrolidin-3-yl}pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | 3-(Pyrrolidin-3-yl)pyridine | HCID 3613651 | — |
| Reactant | 5-Benzyl-4-isoxazolecarboxylic acid | HCID 14787252 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-{1-[(5-Benzylisoxazol-4-yl)carbonyl]pyrrolidin-3-yl}pyridine | HCID 59170231 | 18% |
Reaction Steps
A solution of 5-benzylisoxazole-4-carboxylic acid (10 mg, 0.05 mmol), TBTU (19 mg, 0.06 mmol, 1,2 equ.) and N-ethyl-N-isopropylpropan-2-amine (17 μL, 0.10 mmol, 2 equ) in DMF (0.3 mL) was added to 3-pyrrolidin-3-yl-pyridine (7 mg, 0.05 mmol) and the reaction mixture was left 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 C20H19N3O2: 333.1477, found 333.1477.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07666888B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-887265ccb2ce4ca6b2a0a5f16b1c09c8 |
| Source note | uspto-grants-2010_02 |