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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930128Generated: October 31, 2026

Hydrochloric Acid → 2-(4'-(6-Carbamoyl-3,5-dimethylpyrazin-2-yl)-2,2'-difluorobiphenyl-4-yl)acetic acid

https://huagongshe.com/reaction/1930128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantMethyl 2-(4'-(6-carbamoyl-3,5-dimethylpyrazin-2-yl)-2,2'-difluorobiphenyl-4-yl)acetateHCID 59627685—
Solventtert-ButanolHCID 6386—
Product2-(4'-(6-Carbamoyl-3,5-dimethylpyrazin-2-yl)-2,2'-difluorobiphenyl-4-yl)acetic acidHCID 4984724858.5%

Reaction Conditions

Temperature45 °C

Reaction Steps

Powdered potassium hydroxide (96 mg, 1.71 mmol) was added in one portion to methyl 2-(4′-(6-carbamoyl-3,5-dimethylpyrazin-2-yl)-2,2′-difluorobiphenyl-4-yl)acetate (Intermediate 6-1; 234 mg, 0.57 mmol) in tert-butanol (10 mL) at 45° C. The resulting solution was stirred at 45° C. for 30 minutes, 2M HCl (2 mL) was added and the mixture was evaporated to remove the organic solvent. The suspension was collected by filtration, washed with water (5 mL) and dried under vacuum to afford crude product. The crude product was purified by preparative HPLC (Waters XBridge Prep C18 OBD column, 5μ silica, 50 mm diameter, 150 mm length), using decreasingly polar mixtures of water (containing 0.1% formic acid) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford 2-(4′-(6-carbamoyl-3,5-dimethylpyrazin-2-yl)-2,2′-difluorobiphenyl-4-yl)acetic acid (132 mg, 58.5%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188092B2
Source datasetuspto-grants-2012_05
ORD IDord-1b18896691504c6994f96b645f55b9b9
Source noteuspto-grants-2012_05