HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → HCID 54085301, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | HCID 18349000 | HCID 18349000 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54085301 | HCID 54085301 | 91.5% |
Reaction Steps
To a stirred solution of 4-({3-[2-(tert-butoxycarbonyl-pyridin-4-yl-amino)-ethoxy]-5-chloro-benzoyl}-(2-fluoro-phenyl)-amino)-butyric acid (0.025 g), TBTU (0.028 g) and HOBt (0.012 g) in DMF (1 ml) was added DIPEA (0.015 ml) followed by pyrrolidine (0.007 ml) after 10 min. The reaction mixture was stirred at room temperature for 16 h and then concentrated under reduced pressure. The residue was subjected to preparative hplc and the title compound (0.025 g) was obtained as a colourless gum by concentration of the required fraction under reduced pressure and drying by repetitive addition of acetonitrile and concentration under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06326386B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-ff882d9d784444aab50d7fc41cc18155 |
| Source note | uspto-grants-2001_12 |