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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411162Generated: November 1, 2026

HCID 71252214, compound → HCID 86676755, compound

https://huagongshe.com/reaction/2411162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 71252214HCID 71252214—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 86676755HCID 8667675576.7%

Reaction Steps

To a mixture of methyl 2-bromo-4-nitrobenzoate (871 mg), bis(tricyclohexylphosphine)palladium(II)dichloride (136 mg), tripotassium phosphate (3.98 g) and cyclopropylboronic acid (863 mg) were added toluene (10 mL) and water (0.4 mL), and the mixture was stirred with heating under reflux for 8 hr. The reaction mixture was cooled, water was added, and the mixture was extracted with ethyl acetate. The solvent was evaporated from the organic layer, and the obtained residue was purified by column chromatography (ethyl acetate:hexane) to give methyl 2-cyclopropyl-4-nitrobenzoate (285 mg). The obtained methyl 2-cyclopropyl-4-nitrobenzoate (285 mg) was dissolved in a solution of ethyl acetate and ethanol, and catalytic hydrogenation was performed using palladium carbon to give methyl 4-amino-2-cyclopropylbenzoate (189 mg). Using the obtained methyl 4-amino-2-cyclopropylbenzoate (189 mg) and 3-chloropropane-1-sulfonyl chloride (0.156 mL) and by the reaction and treatment in the same manner as in Preparation Example 17, the title compound (168 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-dba6758934c444c89d335225a3b84717
Source noteuspto-grants-2014_08