HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → N-(6-bromo-2-methoxypyridin-3-yl)formamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 6-Bromo-2-methoxypyridin-3-amine | HCID 10536137 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(6-bromo-2-methoxypyridin-3-yl)formamide | HCID 71492501 | 100% |
Reaction Steps
A mixture of acetic anhydride (8.54 mL, 24.63 mmol) and formic acid (12.8 mL, 24.63 mmol) was stirred at room temperature for 40 min. To this mixture 6-bromo-2-methoxypyridin-3-amine (5.000 g, 24.63 mmol) in 30 mL of THF was added dropwise. The resulting solution was heated at 60° C. with stirring for 16 h. Upon cooling, the reaction mixture was poured into icewater. The resulting precipitate was filtered to give N-(6-bromo-2-methoxypyridin-3-yl)formamide (5.690 g, 24.63 mmol, 100% yield) as light brown solid. LC-MS (M+Na)+=231.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637525B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-6bae5e2d3e7b44ab8d1a5b80af043a77 |
| Source note | uspto-grants-2014_01 |