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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776655Generated: November 3, 2026

Hydrochloric Acid → 2-(N-(tert-butoxycarbonyl)methylsulfonamido)isonicotinic acid

https://huagongshe.com/reaction/1776655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
Reactantethyl 2-(N-(tert-butoxycarbonyl)methyl-sulfonamido)isonicotinateHCID 89460062—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-(N-(tert-butoxycarbonyl)methylsulfonamido)isonicotinic acidHCID 8946005974%

Reaction Steps

To a solution of ethyl 2-(N-(tert-butoxycarbonyl)methylsulfonamido)isonicotinate (0.920 g, 2.67 mmol) in THF (15 ml), aqueous 1M LiOH (2.94 ml, 2.94 mmol) was added, and the reaction was stirred at room temperature for 2 hours. The mixture was diluted with ethyl acetate and acidified with aqueous 2N HCl. The organic layer was separated, washed with brine and dried over Na2SO4. The solvent was removed under vacuum and the solid residue was purified by trituration with iPr2O affording after filtration 2-(N-(tert-butoxycarbonyl)methylsulfonamido) isonicotinic acid as a white solid (0.625 g, 1.976 mmol, 74.0% yield, MS/ESI+ 339.2 [MNa]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265768B2
Source datasetuspto-grants-2016_02
ORD IDord-d2aa593904fd4f47a81a3d35efc731d8
Source noteuspto-grants-2016_02