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HRID 50773생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/50773

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물Diethyl EtherHCID 3283—
반응물4-(Boc-amino)pyridineHCID 9990210—
반응물ButyllithiumHCID 178418339—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물4-{[(Tert-butoxy)carbonyl]amino}pyridine-3-carboxylic acidHCID 2217262354%

반응 조건

온도-78 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713484B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-b4e7f44004264174a2fd5c2c996aaf75
출처 메모uspto-grants-2004_03