HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → Methyl 2-amino-5-((((tert-butoxy)carbonyl)amino)methyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | Methyl 5-tert-butoxycarbonylaminomethyl-2-nitrobenzoate | HCID 19698365 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl 2-amino-5-((((tert-butoxy)carbonyl)amino)methyl)benzoate | HCID 60103040 | 81.1% |
Reaction Steps
A mixture of 0.273 g of methyl 5-{[(tert-butoxycarbonyl)amino]methyl}-2-nitrobenzoate, 0.166 g of ammonium formate and 0.094 g of Pd/C (10%) in 10 ml of EtOH purged beforehand with nitrogen is irradiated under a microwave field at 120° C. for 5 min. The mixture is filtered and the filtrate is evaporated under reduced pressure. The residue is chromatographed on silica gel, elution being carried out with an AcOEt/heptane mixture, (5/95, v/v) as far as (30/70, v/v), to give 0.2 g of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08242126B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-9d2658e95c924ce7af43d372f19f102e |
| Source note | uspto-grants-2012_08 |