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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797216Generated: November 3, 2026

Methylamine → HCID 22176599, compound

https://huagongshe.com/reaction/1797216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant1,4-DioxaneHCID 31275—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 22176530HCID 22176530—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 22176599HCID 2217659925%

Reaction Steps

Into a 50 mL single neck flask, 1 mL oxalyl chloride was added syringe wise to 6-{N-[4-(1-fluoro-1-methyl-2-{[(methylethyl)sulfonyl]amino}ethyl)phenyl]carbamoyl}pyridine-3-carboxylic acid. (110 mg, 0.26 mmol, prepared in example 51) in methylene chloride (10 mL) while stirring under nitrogen at room temperature. Immediately, 1 drop of DMF was added by pipette initiating a foaming of the mixture. The reaction was stirred one hour at this temperature and then concentrated under reduced vacuum to yield a white semi-solid. This material was placed into dioxane (10 mL) and added dropwise to a stirring solution of 40% methylamine in water (3 mL, excess) at room temperature and the mixture was stirred overnight. In the morning, the solution was concentrated under reduced vacuum and the resulting oil was taken into methylene chloride and the organic layer was washed once with H2O, dried over K2CO3, filtered, and concentrated under reduced vacuum to yield 78 mg as an oil. This material was purified via silica gel chromatography employing the chromatotron and using a 1000 micron rotor while eluting with a solvent of ethyl acetate to yield the title compound (28 mg, 25%) as a white solid. Ion spray M.S. 435.2 (M*−1) and 417.1 (M*−19 Fluorine).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034045B1
Source datasetuspto-grants-2006_04
ORD IDord-8aa9e5bad5a244a5afb3cb9304f3c7fb
Source noteuspto-grants-2006_04