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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660917Generated: November 1, 2026

Methylamine → HCID 58835250, compound

https://huagongshe.com/reaction/1660917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantDichloromethaneHCID 6344—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactant4-{[(Tert-butoxy)carbonyl]amino}pyridine-3-carboxylic acidHCID 22172623—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58835250HCID 58835250—

Reaction Conditions

Temperature60 °C

Reaction Steps

The acid, 4-tert-Butoxycarbonylamino-nicotinic acid (1.0 g, 4.20 mmol) was suspended in dry DMF (50 mL) followed by carbonyl-diimidazole (CDI, 1.36 g, 8.40 mmol). The mixture was heated to 60° C. for 1 h, then cooled. Methyl amine in THF was added to the solution followed by evaporation of the mixture. The residue was dissolved in water (20 mL)/chloroform (50 mL) and shaken then the layers separated. The aqueous layer was extracted further with chloroform (3×50 mL) and the combined organic extracts dried (MgSO4) and evaporated to give a yellow oily solid. Silica gel chromatography (CH2Cl2, 0-15% MeOH gradient) gave the desired product, (3-(N-methylaminocarbonyl)-pyridin-4-yl)-carbamic acid tert-butyl ester, as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030318B2
Source datasetuspto-grants-2011_10
ORD IDord-ba0bb7047401424ca8e5cf56ab087375
Source noteuspto-grants-2011_10