HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → (3-Amino-6-bromo-pyrazin-2-yl)-pyridin-3-yl-methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | (3-Amino-pyrazin-2-yl)-pyridin-3-yl-methanone | HCID 68630652 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (3-Amino-6-bromo-pyrazin-2-yl)-pyridin-3-yl-methanone | HCID 86634541 | — |
Reaction Steps
(3-Amino-pyrazin-2-yl)-pyridin-3-yl-methanone (1.00 g, 4.99 mmol) is dissolved in glacial acetic acid (10 ml). Na2CO3 (0.583 g, 5.49 mmol) is added. After evolution of gas has finished, a solution of bromine (0.192 ml, 3.74 mmol) in acetic acid (5 ml) is added dropwise. Na2CO3 (0.583 mg, 5.49 mmol) is added, followed by a second solution of bromine (0.192 ml, 3.74 mmol) in acetic acid (5 ml). The resulting orange suspension is left to stir for 1 hour. The reaction is quenched by pouring onto ice water (150 ml), and the orange solid formed is collected by filtration, washed with water and dried in vacuo at 40° C. overnight to yield the title compound. [M+H]+ 279.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846687B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-2df8dadc6d6444069182564d5bc89b78 |
| Source note | uspto-grants-2014_09 |