HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → Methyl 5-aminopyrazine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Aminopyrazine-2-carbonitrile | HCID 13925294 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 5-aminopyrazine-2-carboxylate | HCID 14536427 | 49% |
Reaction Steps
Reflux a solution of 2.24 g (18.65 mmol) of 5-aminopyrazine-2-carbonitrile and 9.45 mL (74.40 mmol) of boron trifluoride etherate in 50 mL of methanol for 2 h. Concentrate the reaction mixture under reduced pressure and take up the residue obtained in 200 mL of EtOAc and 10 mL of a saturated aqueous solution of NaHCO3. Dry the organic phase over Na2SO4 and concentrate under reduced pressure. Purify the residue obtained by silica gel column chromatography, eluting with a cyclohexane/EtOAc 1:1 mixture. After concentration under reduced pressure, we obtain 1.4 g of methyl 5-aminopyrazine-2-carboxylate in the form of oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552201B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-ac94c59b721c4e578cdf1797aa3cb712 |
| Source note | uspto-grants-2013_10 |