HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-benzyl 3-(ethyl(7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)piperidine-1-carboxylate → (S)-N-ethyl-N-(piperidin-3-yl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-benzyl 3-(ethyl(7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)piperidine-1-carboxylate | HCID 86706456 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (S)-N-ethyl-N-(piperidin-3-yl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine | HCID 118906729 | 61.8% |
Reaction Steps
A mixture of (S)-benzyl 3-(ethyl(7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)piperidine-1-carboxylate (130 mg, 0.243 mmol), 10% Pd/C (130 mg) in ethanol (4 mL) was placed under an atmosphere of hydrogen (1 atm) for 1 h. The reaction mixture was filtered through a celite pad and the filtrate was concentrated in vacuo to yield the title intermediate (60 mg, 61%). LC-MS: m/z [M+1]=400.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273028B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-958e54f5e6e74b5087f0af092c294d70 |
| Source note | uspto-grants-2016_03 |