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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541552Generated: October 31, 2026

Acetic Acid → HCID 86705126, compound

https://huagongshe.com/reaction/541552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetoneHCID 180—
ReactantSodium IodideHCID 5238—
ReactantCesium carbonateHCID 10796—
ReactantDiisopropylethylamineHCID 81531—
ReactantChloromethyl isopropyl carbonateHCID 14787051—
ReactantHCID 178521475HCID 178521475—
CatalystZincHCID 23994—
ProductHCID 86705126HCID 8670512619.1%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of chloromethyl isopropyl carbonate (15.6 mg, 102 μmol) and NaI (15.3 mg, 102 μmol) in acetone (0.7 mL, 10 mmol) was stirred at 65° C. for 1 hour, then added (R)-3-[N-(3′-chlorobiphenyl-4-ylmethyl)-N′-(3-hydroxyisoxazole-5-carbonyl)hydrazino]-2-hydroxypropionic acid 2-oxo-2-phenylethyl ester (20.0 mg, 36.4 μmol) that had been dissolved in acetone (0.4 mL, 5 mmol) at room temperature and treated with cesium carbonate (13.0 mg, 40 μmol). The resulting mixture was then heated at 40° C. for 1 hour. DIPEA (0.2 mL, 1 mmol) was added and heating continued for 1 hour. The mixture was cooled to room temperature and concentrated. The residue was partitioned between EtOAc (10.0 mL) and water (2.0 mL). The organic layer was washed with saturated aqueous NaHCO3 (3.0 mL), saturated aqueous NaCl (3.0 mL), dried over Na2SO4, filtered, and concentrated. Zinc 90.8 mg, 1.4 mmol) and AcOH (0.5 mL, 9 mmol) were added and the resulting mixture was stirred at room temperature for 1 hour. The solids were washed with AcOH (1.0 mL) then filtered. The filtrates were combined and purified by reverse phase preparative HPLC to yield the title compound (3.8 mg). MS m/z [M+H]+ calc'd for C25H26ClN3O9, 548.14. found 548.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871792B2
Source datasetuspto-grants-2014_10
ORD IDord-97e85896bde443e6bf2fd339dc4d96f3
Source noteuspto-grants-2014_10