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Triethylsilane → 4-Fluoro-3-{[2-(pyridin-2-ylamino)-thiazol-5-ylmethyl]-amino}-benzoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylsilane | HCID 12052 | — |
| 反応物 | 3-Amino-4-fluorobenzoic acid | HCID 75396 | — |
| 反応物 | 2-(Pyridin-2-ylamino)thiazole-5-carbaldehyde | HCID 22019058 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-Fluoro-3-{[2-(pyridin-2-ylamino)-thiazol-5-ylmethyl]-amino}-benzoic acid | HCID 22019056 | 91.3% |
反応手順
To a suspension of 2-(pyridin-2-ylamino)-thiazole-5-carbaldehyde (1.0 g, 4.90 mmol, compound 1A) in methylene chloride (20 mL) at RT 3-amino-4-fluorobenzoic acid (0.95 g, 4.90 mmol) TFA (5 mL) and triethylsilane (1.71 mg, 14.7 mmol) were added. The above reaction mixture was stirred at RT for 4 h, then concentrated in vacuo and the resulting slurry was triturated with methanol to afford 4-fluoro-3-{[2-(pyridin-2-ylamino)-thiazol-5-ylmethyl]-amino}-benzoic acid as light yellow solid (1.54 g, 91%) (M+H)+=345.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07084160B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-dcdd4dc25d754501bcc4494e4162c584 |
| 出典メモ | uspto-grants-2006_08 |