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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941895Generated: October 30, 2026

Sodium Acetate → HCID 58504354, compound

https://huagongshe.com/reaction/1941895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
ReactantHCID 58504345HCID 58504345—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 58504354HCID 5850435471.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a suspension of (Z)-methyl 1-(4-(N′-(5-amino-1-phenyl-1H-pyrazole-4-carbonyloxy)carbamimidoyl)benzyl)azetidine-3-carboxylate (102 mg, 0.227 mmol) in EtOH (3 mL) was added sodium acetate (37.3 mg, 0.455 mmol) as a solution in water (1 mL). The mixture was heated to 90° C. for 3 hr. The reaction mixture was transferred to a microwave vial and was then heated to 120° C. for 30 minutes. The reaction mixture was partitioned between EtOAc (30 mL) and water (30 mL). The aqueous layer was extracted with EtOAc (15 mL) and the combined organic layers were dried (MgSO4) and concentrated to afford an oil that was chromatographed on a 12 gm Isco silica gel cartridge, eluting with a 0-100% EtOAc/hexane gradient. The pure fractions were concentrated to afford methyl 1-(4-(5-(5-amino-1-phenyl-1H-pyrazol-4-yl)-1,2,4-oxadiazol-3-yl)benzyl)azetidine-3-carboxylate (70 mg, 0.163 mmol) as a colorless oil. HPLC retention time=1.35 (ethyl ester-1.42) minutes (PHENOMENEX® Luna 4.6×30 mm S-5 ODS column) eluting with 10-90% aqueous methanol+0.1% TFA over a 2 minute gradient. MS:(M+H)=431.23 (ethyl ester-445.25). (The product is a mixture of methyl ester and ethyl ester due to partial transesterification during the reaction. The mixture was carried on through the sequence.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389509B2
Source datasetuspto-grants-2013_03
ORD IDord-4199751dc38e42fabbaccd95acd7f3fd
Source noteuspto-grants-2013_03