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Tetrahydrofuran → 4-(4-Bromo-2-fluorophenylamino)-6-chloro-5-fluoro-nicotinic acid methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Trimethylsilyldiazomethane | HCID 167693 | — |
| 反応物 | 4-(4-Bromo-2-fluorophenylamino)-6-chloro-5-fluoro-nicotinic acid | HCID 86601526 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 4-(4-Bromo-2-fluorophenylamino)-6-chloro-5-fluoro-nicotinic acid methyl ester | HCID 86601527 | 92.3% |
反応手順
A hexanes solution of TMSCH2N2 (9.46 mL, 18.9 mmol) was added to 4-(4-bromo-2-fluorophenylamino)-6-chloro-5-fluoro-nicotinic acid (4.59 g, 12.62 mmol) in a solution of 3:1 THF:MeOH (48 mL) at 0° C. The reaction mixture was warmed to room temperature and stirred for 1 hour. After quenching with AcOH, the reaction mixture was diluted with ethyl acetate and water. The layers were separated and the organic layer was washed with water, saturated NaHCO3 solution and brine. The organic layer was dried (MgSO4) and concentrated to give 4.40 g (92%) clean desired product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08101639B2 |
| 出典データセット | uspto-grants-2012_01 |
| ORD ID | ord-5794dbd62abe482d8058c47f8cb4444f |
| 出典メモ | uspto-grants-2012_01 |