Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930112Generated: October 26, 2026

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

https://huagongshe.com/reaction/1930112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl 2-(4'-(6-carbamoyl-3,5-dimethylpyrazin-2-yl)-2-chloro-5-methylbiphenyl-4-yl)acetateHCID 59627700—
Solventtert-ButanolHCID 6386—
Product2-(4'-(6-Carbamoyl-3,5-dimethylpyrazin-2-yl)-2-chloro-5-methylbiphenyl-4-yl)acetic acidHCID 4984717490.6%

Reaction Conditions

Temperature55 °C

Reaction Steps

Powdered potassium hydroxide (88 mg, 1.56 mmol) was added in one portion to ethyl 2-(4′-(6-carbamoyl-3,5-dimethylpyrazin-2-yl)-2-chloro-5-methylbiphenyl-4-yl)acetate (Intermediate 3-1; 228 mg, 0.52 mmol) in tert-butanol (15 mL) at 55° C. The resulting mixture was stirred at 55° C. for 45 minutes, 2M HCl (˜1 mL) was added and the mixture was evaporated to remove the organic solvent. The suspension was collected by filtration, washed with water (20 mL) and air dried to afford crude product as a pale yellow solid, which contained a minor impurity. 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-chloro-5-methylbiphenyl-4-yl)acetic acid (193 mg, 90%) as a cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188092B2
Source datasetuspto-grants-2012_05
ORD IDord-612e90f634fb4134a180780308803bcc
Source noteuspto-grants-2012_05