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HRID 422765作成日:2026年10月25日

Tetrahydrofuran → 4-(4-Bromo-2-fluorophenylamino)-6-chloro-5-fluoro-nicotinic acid methyl ester

https://huagongshe.com/reaction/422765

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物TrimethylsilyldiazomethaneHCID 167693—
反応物4-(4-Bromo-2-fluorophenylamino)-6-chloro-5-fluoro-nicotinic acidHCID 86601526—
溶媒MethanolHCID 887—
生成物4-(4-Bromo-2-fluorophenylamino)-6-chloro-5-fluoro-nicotinic acid methyl esterHCID 8660152792.3%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101639B2
出典データセットuspto-grants-2012_01
ORD IDord-5794dbd62abe482d8058c47f8cb4444f
出典メモuspto-grants-2012_01