HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → {(4R)-4-phenyl-1-[(5-pyridin-2-ylisoxazol-4-yl)carbonyl]pyrrolidin-3-yl}methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | (4-Phenylpyrrolidin-3-yl)methanol | HCID 13316928 | — |
| Reactant | 5-(Pyridin-2-yl)-1,2-oxazole-4-carboxylic acid | HCID 22309070 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | {(4R)-4-phenyl-1-[(5-pyridin-2-ylisoxazol-4-yl)carbonyl]pyrrolidin-3-yl}methanol | HCID 68683047 | 26% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07666888B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-455bdb12276c450c81f770d057345e5c |
| Source note | uspto-grants-2010_02 |