HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930149Generated: October 29, 2026
Potassium Hydroxide → HCID 67285555, compound
https://huagongshe.com/reaction/1930149
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 67762760 | HCID 67762760 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 67285555 | HCID 67285555 | 9.59% |
Reaction Steps
Potassium hydroxide (70.3 mg, 1.25 mmol) was added in one portion to (S)-ethyl 2-(2-(4′-(6-carbamoyl-3,5-dimethylpyrazin-2-yl)-2-chlorobiphenyl-4-yl)acetamido)-4-methylpentanoate (Intermediate 15-1; 224.4 mg, 0.42 mmol) in t-BuOH (2696 μL) at RT. The resulting solution was stirred at 45° C. for 5 hours a precipitate formed. The reaction mixture was quenched with 2M HCl (5 mL), The reaction mixture was evaporated to dryness and redissolved in water (10 mL), and filtered through nylon, washed with water and dried under vacuum. 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 (S)-2-(2-(4′-(6-carbamoyl-3,5-dimethylpyrazin-2-yl)-2-chlorobiphenyl-4-yl)acetamido)-4-methylpentanoic acid (20.40 mg, 9.59%) as a white 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-68c49c0f56154b4cb04cf6c03218262c |
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| Source note | uspto-grants-2012_05 |
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