HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 118037920, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 118037594 | HCID 118037594 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 118037920 | HCID 118037920 | — |
Reaction Steps
A mixture of tert-butyl 4-(3-ethyl-2-oxo-4-(((trifluoromethyl)sulfonyl)oxy)pyridin-1(2H)-yl)piperidine-1-carboxylate (1.14 g), triethylamine (0.699 mL), methanol (3.05 mL), 1,1′-bis(diphenylphosphino)ferrocene-palladium(II) dichloride (0.184 g), and DMF (12.5 mL) was stirred at 90 C for 4 hours in a carbon monooxide atmosphere of 0.5 MPa. Water was added to the reaction mixture, followed by extraction with ethyl acetate twice. The obtained organic layer was washed with saturated saline twice and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (NH, hexane/ethyl acetate) to obtain the title compound (0.798 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120777B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-cf934c268edc486da59063d09db34382 |
| Source note | uspto-grants-2015_09 |