HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → Carbamic acid, [6-[(4-aminobenzoyl)amino]hexyl]-, 1,1-dimethylethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 58720809 | HCID 58720809 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Carbamic acid, [6-[(4-aminobenzoyl)amino]hexyl]-, 1,1-dimethylethyl ester | HCID 58720810 | 105.3% |
Reaction Steps
The above amide (265 mg, 0.750 mmol) was dissolved in EtOH (25 mL). The reaction mixture was charged with ammonium formate (500 mg) and 10% palladium on carbon (100 mg) and stirred for 4 days at ambient temperature. The reaction was filtered through diatomaceous earth and concentrated to recover 265 mg of [6-(4-amino-benzoylamino)-hexyl]-carbamic acid tert-butyl ester as a white crystalline solid (quantitative yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07588899B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-ef9040cae8ba4599ac2e204884e49b07 |
| Source note | uspto-grants-2009_09 |