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Triethylamine → Methyl 5-bromopyrimidine-2-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Sulfuryl chloride | HCID 24648 | — |
| 反応物 | 5-Bromopyrimidine-2-carboxylic acid | HCID 16462970 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Methyl 5-bromopyrimidine-2-carboxylate | HCID 45790831 | — |
反応手順
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+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07977372B2 |
| 出典データセット | uspto-grants-2011_07 |
| ORD ID | ord-19c777ff27fe4c4f8e4625c32492bb88 |
| 出典メモ | uspto-grants-2011_07 |