HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 21922598, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Toluene-p-sulphonic anhydride | HCID 77773 | — |
| Reactant | HCID 21922792 | HCID 21922792 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21922598 | HCID 21922598 | 53.4% |
Reaction Steps
1.99 g (6.09 mmol) of p-toluenesulfonic anhydride and 0.85 ml (6.09 mmol) of triethylamine were added to a solution of 1.64 g (5.53 mmol) of 3-(4-fluorophenyl)-1-(3-hydroxypropyl)-2-(pyridin-4-yl)-1H-pyrrole [prepared as described in step 22(ii) above] in 16 ml of dichloromethane. The resulting mixture was stirred at room temperature for 2 hours, after which the solvent was distilled off by evaporation under reduced pressure. The resulting residue was purified by chromatography on a silica gel column using a 1:1 by volume mixture of hexane and ethyl acetate as the eluant to afford 1.33 g (yield 53%) of the title compound as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07122666B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-4b3a2302b9eb47a1a44a2df5539c80fd |
| Source note | uspto-grants-2006_10 |