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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873537Generated: October 30, 2026

Citric Acid → HCID 117700524, compound

https://huagongshe.com/reaction/873537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantMethanesulfonamideHCID 72879—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 78324914HCID 78324914—
SolventDimethylformamideHCID 6228—
ProductHCID 117700524HCID 11770052442.1%

Reaction Steps

1,1′-Carbonyldiimidazole (104 mg, 0.64 mmol) was added to a solution of the 3-ethyl-6-[4-methoxy-2-methyl-3-(3,3,6,6-tetramethyl-1,8-dioxo-2,3,4,5,6,7,8,9-octahydro-1H-xanthen-9-yl)phenyl]pyridine-2-carboxylic acid produced in Example 13 (267 mg, 0.49 mmol) in DMF (5.3 ml) at room temperature, and the mixture thus obtained was then stirred at the same temperature as above for 1.5 hours. Thereafter, methanesulfonamide (60.7 mg, 0.64 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (0.096 ml, 0.64 mmol) were added to the resulting solution at room temperature, and the mixture thus obtained was then stirred at the same temperature as above for 3 hours. Thereafter, an aqueous solution of citric acid (472 mg, 2.46 mmol) was added to the reaction solution, and the mixed solution was then extracted with ethyl acetate. The organic layer thus obtained was washed with water, and was then dried over anhydrous sodium sulfate. The solvent was distilled away under reduced pressure, and the residue thus obtained was then purified by silica gel column chromatography (methanol:dichloromethane=0:1 to 1:9, v/v). The solid thus obtained was washed with diethyl ether, followed by collection by filtration and drying, to obtain the title compound (128 mg, yield: 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975263B2
Source datasetuspto-grants-2015_03
ORD IDord-324fe58ac9374e2db94895af2432c695
Source noteuspto-grants-2015_03