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HRID 6879作成日:2026年10月24日

Triethylsilane → 4-Fluoro-3-{[2-(pyridin-2-ylamino)-thiazol-5-ylmethyl]-amino}-benzoic acid

https://huagongshe.com/ja/reaction/6879

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylsilaneHCID 12052—
反応物3-Amino-4-fluorobenzoic acidHCID 75396—
反応物2-(Pyridin-2-ylamino)thiazole-5-carbaldehydeHCID 22019058—
溶媒DichloromethaneHCID 6344—
生成物4-Fluoro-3-{[2-(pyridin-2-ylamino)-thiazol-5-ylmethyl]-amino}-benzoic acidHCID 2201905691.3%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084160B2
出典データセットuspto-grants-2006_08
ORD IDord-dcdd4dc25d754501bcc4494e4162c584
出典メモuspto-grants-2006_08