HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Amino-6-bromo-3-nitro-pyridin-4-yl)-benzyl-carbamic acid ethyl ester → HCID 86614490, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Amino-6-bromo-3-nitro-pyridin-4-yl)-benzyl-carbamic acid ethyl ester | HCID 86614485 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86614490 | HCID 86614490 | 36.2% |
Reaction Steps
(2-Amino-6-bromo-3-nitro-pyridin-4-yl)-benzyl-carbamic acid ethyl ester (50 mg, 0.13 mmol) was dissolved in AcOH (3 ml). Fe powder (43 mg, 0.76 mmol) was added and the mixture was vigorously stirred at room temperature for 24 h. The reaction mixture diluted with EtOAc (20 ml) and water (10 ml). The mixture was filtered through celite, washing through with EtOAc (20 ml). The layers were separated and the organic layer was washed with water (10 ml), sat. NaHCO3 (aq) (2×10 ml) and brine (10 ml), dried over MgSO4 and concentrated in vacuo. The crude was triturated in pentane, filtered and dried in vacuo at 40° C. to give the title compound (15 mg) as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691877B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-30cdc55b88e345469bdb971dedba6230 |
| Source note | uspto-grants-2010_04 |