HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → Methyl 5-bromo-2-isopropylpyrimidine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Bromo-2-(propan-2-yl)pyrimidine-4-carboxylic acid | HCID 67299898 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 5-bromo-2-isopropylpyrimidine-4-carboxylate | HCID 67299889 | 94% |
Reaction Steps
To a stirred, cooled (0° C.) solution of 5-bromo-2-isopropyl-pyrimidine-4-carboxylic acid (3 g, 12.2 mmol) in methanol (50 ml) under an argon atmosphere was added dropwise thionyl chloride (4.37 g, 2.68 ml, 36.7 mmol). When the addition was complete, the mixture was allowed to warm to r.t. and stirring at r.t. was continued for 17 h. The orange mixture was concentrated to leave a paste which was taken up in EtOAc (50 ml)/saturated aqueous Na2CO3 solution (50 ml). The aqueous phase was extracted with EtOAc. The combined organics were washed with H2O and brine, dried over MgSO4, filtered and concentrated to leave the product (2.98 g, 94%) as a light brown oil which was used in the next reaction step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08470820B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-16ef6c0f88be4cc8b6d41501b60a2d55 |
| Source note | uspto-grants-2013_06 |