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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386143Generated: November 1, 2026

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

https://huagongshe.com/reaction/1386143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantDiethyl EtherHCID 3283—
Reactant4-(Boc-amino)pyridineHCID 9990210—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-{[(Tert-butoxy)carbonyl]amino}pyridine-3-carboxylic acidHCID 2217262354%

Reaction Conditions

Temperature-78 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265410B1
Source datasetuspto-grants-2001_07
ORD IDord-d1266d8651e44b3e9baba8077459cfa5
Source noteuspto-grants-2001_07