HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 5-bromopyrimidine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 5-Bromopyrimidine-2-carboxylic acid | HCID 16462970 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 5-bromopyrimidine-2-carboxylate | HCID 45790831 | — |
Reaction Steps
To a solution of 5-bromo-2-pyrimidine carboxylic acid (6 g, 29.6 mmol) in MeOH (300 mL) was added Et3N (5.98 g, 59.2 mmol). The mixture was cooled to 0 degrees Celsius, and sulfonyl chloride (5.3 g, 44.4 mmol) was added dropwise to the solution. After addition, the mixture was stirred at rt for 12 hours. The solvent was removed and the residue was dissolved in ethyl acetate. The organic layer was washed with sodium bicarbonate, brine, and dried with sodium sulfate. The solvent was removed to give the pure product. MS: calc'd 217 (MH+), exp 217 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977372B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-19c777ff27fe4c4f8e4625c32492bb88 |
| Source note | uspto-grants-2011_07 |