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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930141Generated: October 31, 2026

Methanol → Methyl 1-(4'-(6-carbamoyl-3,5-dimethylpyrazin-2-yl)-2-chlorobiphenyl-4-yl)cyclopropanecarboxylate

https://huagongshe.com/reaction/1930141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantMethyl 1-(3-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropane-1-carboxylateHCID 59627717—
Reactant4-(6-Carbamoyl-3,5-dimethylpyrazin-2-yl)phenyl trifluoromethanesulfonateHCID 59627729—
CatalystHCID 178418807HCID 178418807—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductMethyl 1-(4'-(6-carbamoyl-3,5-dimethylpyrazin-2-yl)-2-chlorobiphenyl-4-yl)cyclopropanecarboxylateHCID 5962766749.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 4-(6-carbamoyl-3,5-dimethylpyrazin-2-yl)phenyl trifluoromethanesulfonate (Intermediate 7-4; 245 mg, 0.65 mmol) and methyl 1-(3-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropanecarboxylate (Intermediate 10-2; 220 mg, 0.65 mmol) and potassium phosphate, tri-basic (166 mg, 0.78 mmol) in DME (4 mL), methanol (2 mL) and water (1 mL) was thoughroughly degassed. The mixture was treated with PdCl2(dppf)-DCM adduct (26.7 mg, 0.03 mmol), degassed again and the atmosphere replaced with nitrogen before being heated to 90° C. for 4 hours in the microwave. The reaction mixture was allowed to cool to room temperature and then evaporated. The crude product was partitioned between EtOAc (75 mL), and saturated brine (75 mL). The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 70% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford methyl 1-(4′-(6-carbamoyl-3,5-dimethylpyrazin-2-yl)-2-chlorobiphenyl-4-yl)cyclopropanecarboxylate (141 mg, 49.5%) as a colourless gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188092B2
Source datasetuspto-grants-2012_05
ORD IDord-b3aaec71b9b84addaf4cb48a88887d0b
Source noteuspto-grants-2012_05