戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 50773作成日:2026年10月27日

Carbon Dioxide → 4-{[(Tert-butoxy)carbonyl]amino}pyridine-3-carboxylic acid

https://huagongshe.com/reaction/50773

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物Diethyl EtherHCID 3283—
反応物4-(Boc-amino)pyridineHCID 9990210—
反応物ButyllithiumHCID 178418339—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物4-{[(Tert-butoxy)carbonyl]amino}pyridine-3-carboxylic acidHCID 2217262354%

反応条件

温度-78 °C

反応手順

n-Butyl lithium (2.18 M, 24 mL, 52.51 mmol) is added slowly to a solution of 4-(N-t-butoxycarbonylamino)-pyridine (4.08 g, 21 mmol) in THF (50 mL, stirred under N2 at −78° C. The solution is allowed to warm to 0° C., stirred for 3 h, then cooled again to −78° C. and poured into ether (100 mL) containing dry ice. The solution is warmed to room temperature with constant stirring. Water is added and the mixture is neutralized with acetic acid. The resulting solid is collected by vacuum filtration and dried in a vacuum oven to give 4-(N-t-butoxycarbonylamino)nicotinic acid (2.72 g, 54%) as a brown solid. 1H NMR (DMSO) δ 11.75 (1H, brs), 8.95 (1H, s), 8.50 (1H, d, J=6.0 Hz) 8.20 (1H, d, J=6.0 Hz), 1.49 (9H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713484B2
出典データセットuspto-grants-2004_03
ORD IDord-b4e7f44004264174a2fd5c2c996aaf75
出典メモuspto-grants-2004_03