Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541550Generated: October 31, 2026

Acetic Acid → HCID 117669084, compound

https://huagongshe.com/reaction/541550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
ReactantChloromethyl butanoateHCID 2725008—
ReactantHCID 178521475HCID 178521475—
CatalystZincHCID 23994—
SolventAcetoneHCID 180—
ProductHCID 117669084HCID 1176690848.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of chloromethyl butyrate (20.5 μL, 164 μmol) and NaI (24.5 mg, 164 μmol) in acetone (2.0 mL, 27 mmol) was stirred at 60° C. for 1 hour, then cooled to room temperature and added to a mixture of (R)-3-[N-(3′-chlorobiphenyl-4-ylmethyl)-N′-(3-hydroxyisoxazole-5-carbonyl)hydrazino]-2-hydroxypropionic acid 2-oxo-2-phenylethyl ester (30.0 mg, 54.5 μmol) and Et3N (38.0 μL, 273 μmol) in acetone (1 mL). The resulting mixture was stirred at room temperature for 2 hours, concentrated, dissolved in AcOH (2 mL), filtered, and purified by reverse phase preparative HPLC. The desired fractions were combined and lyophilized. Zinc (178 mg, 2.7 mmol) and AcOH (1.0 mL, 18 mmol) was added and the resulting mixture was stirred at room temperature for 2 hours. The mixture was filtered and purified by reverse phase preparative HPLC to yield the title compound (2.5 mg). MS m/z [M+H]+ calc'd for C25H26ClN3O8, 532.14. found 532.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871792B2
Source datasetuspto-grants-2014_10
ORD IDord-f0794b99defb45808dfe5c8a81f9ec0b
Source noteuspto-grants-2014_10