HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 59332343, compound → tert-Butyl 4-(3-aminopyridin-4-yl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 59332343 | HCID 59332343 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethylacetate methanol | HCID 21584119 | — |
| Product | tert-Butyl 4-(3-aminopyridin-4-yl)piperazine-1-carboxylate | HCID 43462405 | — |
Reaction Steps
The 4-(3-nitro-pyridin-4-yl)-piperazine-1-carboxylic acid tert-butyl ester (633 mg) was then diluted with MeOH/EtOAc (1:1, 10 mL) and to the resulting solution was added Pd on carbon (5% Pd). The resulting reaction mixture was stirred under a hydrogen atmosphere at room temperature for about 15 hours. The reaction mixture was filtered through a pad of celite and the filtrate was concentrated in vacuo to provide 4-(3-amino-pyridin-4-yl)-piperazine-1-carboxylic acid tert-butyl ester as a solid form. HPLC-MS RT=1.10 min, mass calculated for formula C14H22N4O2 278.17, observed LCMS m/z 279.28 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318735B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-b7c8822e214f4c60967948f2989b740b |
| Source note | uspto-grants-2012_11 |