HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-butyl 4-(2-(N-methoxy-N-methylcarbamoyl)-6-fluorophenyl)-5,6-dihydropyridine-1(2H)-carboxylate → tert-Butyl 4-(2-(N-methoxy-N-methylcarbamoyl)-6-fluorophenyl)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-butyl 4-(2-(N-methoxy-N-methylcarbamoyl)-6-fluorophenyl)-5,6-dihydropyridine-1(2H)-carboxylate | HCID 57774426 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl 4-(2-(N-methoxy-N-methylcarbamoyl)-6-fluorophenyl)piperidine-1-carboxylate | HCID 57774380 | — |
Reaction Steps
A solution of tert-butyl 4-(2-(N-methoxy-N-methylcarbamoyl)-6-fluorophenyl)-5,6-dihydropyridine-1(2H)-carboxylate (450 mg, 1.235 mmol) and PtO2 (180 mg) in EtOH (19 mL) was shaken in a Parr flask for 1 h15 under 51 psi of H2. The reaction was monitored by LC/MS. Unreacted SM was detected, so another 150 mg of PtO2 (total: 450 mg, 30 wt %) was then added and the mixture was hydrogenated under 50 psi for another 3 h. Mostly desired product was detected after 4 h by LC/MS (Rt=2.83 min). The catalyst was filtered off and the solution was concentrated in vacuo to yield 435 mg of tert-butyl 4-(2-(N-methoxy-N-methylcarbamoyl)-6-fluorophenyl)piperidine-1-carboxylate as a clear thick oil which was used as is for the next step. LC/MS ES+1: 367.38.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163737B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-086d53ecf2bb4e56bdc4a8d37d640eec |
| Source note | uspto-grants-2012_04 |