戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1441646作成日:2026年10月27日

Lithium Chloride → 2-Amino-5-pyrazin-2-yl-4-trifluoromethyl-benzoic acid methyl ester

https://huagongshe.com/reaction/1441646

反応式

関与物質

役割名称HCID仕込み量
反応物Lithium ChlorideHCID 433294—
反応物2-(Tributylstannyl)pyrazineHCID 2737316—
反応物Phenol, bis(1,1-dimethylethyl)-4-methyl-HCID 3034427—
反応物Methyl 2-amino-5-iodo-4-(trifluoromethyl)benzoateHCID 53436880—
触媒HCID 178418397HCID 178418397—
溶媒1,4-DioxaneHCID 31275—
生成物2-Amino-5-pyrazin-2-yl-4-trifluoromethyl-benzoic acid methyl esterHCID 1196578238.4%

反応条件

温度120 °C

反応手順

A solution containing 2-amino-5-iodo-4-trifluoromethyl-benzoic acid methyl ester (750 mg, 2.17 mmol), 2-tributylstannylpyrazine (1.0 g, 2.7 mmol) and (Ph3P)4Pd (125.6 mg, 0.109 mmol) in dioxane (40 mL) was heated at 120° C. for 17 h. LiCl (276.4 mg, 6.5 mmol) was added and the reaction mixture was refluxed for 1.5 h prior to the addition of di-t-butyl-p-cresol (188 mg, 0.85 mmol) and another portion of (Ph3P)4Pd (251.2 mg, 0.22 mmol). Heating was continued for 16 h, for a total reaction time of 36 h. After cooling to r.t., the solvent was removed in vacuo and the residue was purified by flash chromatography (200 g silica gel, hexanes→EtOAc:hexanes (3:7 to 1:1)). The fractions containing the product were combined and concentrated in vacuo. The resultant oil was further purified by partitioning between CH3CN and hexanes. The acetonitrile layer was concentrated in vacuo to furnish the title compound (248 mg, 38%) as a solid. API-ES: m/z 298 [M+H]+, rt 4.18 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07655666B2
出典データセットuspto-grants-2010_02
ORD IDord-ddf1725357c042f9bab24c11b03981ce
出典メモuspto-grants-2010_02