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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797186Generated: November 1, 2026

Methylamine → HCID 9930416, compound

https://huagongshe.com/reaction/1797186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant1,4-DioxaneHCID 31275—
ReactantOxalyl chlorideHCID 65578—
Reactant4-[4-(1-fluoro-1-methyl-2-{[(methylethyl)sulfonyl]amino}ethyl)phenyl]benzoic AcidHCID 22176583—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 9930416HCID 993041649%

Reaction Steps

Into a 50 mL single neck flask, 1 mL oxalyl chloride was added syringe wise to (−)-4-[4-(1-fluoro-1-methyl-2-{[(methylethyl)sulfonyl]amino}ethyl)phenyl]benzoic acid (300 mg, 0.79 mmol, prepared in example 1a) in methylene chloride (15 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 (20 mL) and added dropwise to a stirring solution of 40% methylamine (5 mL) 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 391 mg as a solid. This material was purified via recrystallization from hexane/ethyl acetate 1:1 to yield the title compound (231 mg, 49%) as a white solid. Ion spray M.S. 391.4 (M*−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034045B1
Source datasetuspto-grants-2006_04
ORD IDord-7ac3b3a19dc749bbbbc6211b17ce5339
Source noteuspto-grants-2006_04