戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 454768作成日:2026年10月26日

Citric Acid → Tert-butyl 4-(4-((tert-butoxycarbonyl)(methyl)amino)phenyl)-2-(5-phenylpyridine-3-carboxamido)benzoate

https://huagongshe.com/reaction/454768

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物Sodium CarbonateHCID 10340—
反応物tert-Butyl methyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamateHCID 4712653—
反応物Tert-butyl 4-bromo-2-(5-phenylpyridine-3-carboxamido)benzoateHCID 58508430—
触媒HCID 178418476HCID 178418476—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
溶媒Ethyl AcetateHCID 8857—
生成物Tert-butyl 4-(4-((tert-butoxycarbonyl)(methyl)amino)phenyl)-2-(5-phenylpyridine-3-carboxamido)benzoateHCID 6699030083.4%

反応手順

Water (0.60 mL), sodium carbonate (88 mg), tert-butyl methyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate (0.13 g), and bis(triphenylphosphine)palladium(II) dichloride (5.0 mg) were added to an ethylene glycol dimethyl ether (2.0 mL) solution of tert-butyl 4-bromo-2-(5-phenylpyridine-3-carboxamido)benzoate (0.15 g), followed by heating to reflux under a nitrogen atmosphere for 1 hour. The reaction mixture was cooled to room temperature, and then a 10% aqueous solution of citric acid and ethyl acetate were added thereto. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [eluent: 95-85% hexane/ethyl acetate] to obtain 0.16 g of tert-butyl 4-(4-((tert-butoxycarbonyl)(methyl)amino)phenyl)-2-(5-phenylpyridine-3-carboxamido)benzoate as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08492582B2
出典データセットuspto-grants-2013_07
ORD IDord-66c81f6e2ef04674afc77253705b5802
出典メモuspto-grants-2013_07