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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926004Generated: November 1, 2026

Ethyl 3-aminobenzoate → HCID 57597372, compound

https://huagongshe.com/reaction/1926004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-aminobenzoateHCID 11400—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantSodium BicarbonateHCID 516892—
Reactant4-chloro-5H-pyrrolo[3,2-d]pyrimidineHCID 5370695—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 57597372HCID 5759737255.8%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 4-chloro-5H-pyrrolo[3,2-d]pyrimidine (2.78 g), ethyl 3-aminobenzoate (4.49 g) and 1-methyl-2-pyrrolidone (20 mL) was stirred at 120° C. for 1.5 hrs. To the reaction mixture were added ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution. The insoluble material was filtered off, and the ethyl acetate layer was separated. The aqueous layer was extracted with ethyl acetate, and the mixed ethyl acetate layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The filtered insoluble material was suspended in methanol and ethyl acetate and saturated brine were added. The ethyl acetate layer was separated. The ethyl acetate layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The mixed ethyl acetate layer was concentrated under reduced pressure and the obtained residue was purified by silica gel column chromatography (eluent, ethyl acetate) and crystallized from methanol-acetone-diisopropyl ether to give the title compound (2.85 g) as a pale-brown powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178543B2
Source datasetuspto-grants-2012_05
ORD IDord-373316a2448b496ab04c7c5b1cafdec2
Source noteuspto-grants-2012_05