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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 2-(4'-(6-carbamoyl-3,5-dimethylpyrazin-2-yl)-2-chloro-5-methylbiphenyl-4-yl)acetate | HCID 59627700 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2-(4'-(6-Carbamoyl-3,5-dimethylpyrazin-2-yl)-2-chloro-5-methylbiphenyl-4-yl)acetic acid | HCID 49847174 | 90.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188092B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-612e90f634fb4134a180780308803bcc |
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| Source note | uspto-grants-2012_05 |
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