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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642763Generated: November 2, 2026

1,2-Dichloroethane → HCID 58017527, compound

https://huagongshe.com/reaction/1642763

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantLithium HydroxideHCID 3939—
Reactant4-MethylmorpholineHCID 7972—
ReactantHCID 57473410HCID 57473410—
ReactantHCID 58017546HCID 58017546—
ReactantHCID 178418300HCID 178418300—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 58017527HCID 5801752787.3%

Reaction Steps

To a solution of 2-tert-butyl 3-ethyl (3S)-isoxazolidine-2,3-dicarboxylate (245 mg, 1.00 mmol) in acetonitrile (2.5 mL) and water (1 mL) was added lithium hydroxide (1 M in water, 1.00 mL, 1.00 mmol) and the mixture was stirred at rt for 30 min. To this solution was added 5-chloro-2-tetrazol-1-yl-benzylamine hydrochloride (295 mg, 1.20 mmol, prepared as described in J. Med. Chem. 2004, 47, 2995), hydroxybenzotriazole (135 mg, 1.00 mmol, as a 20% solution in water, ca 0.65 mL), EDC (288 mg, 1.50 mmol) and NMM (202 mg, 2.00 mmol). The resulting mixture was stirred at rt over night, then diluted with DCM and washed with 1 M HCl and saturated sodium hydrogen carbonate. The organic phase was dried, filtered, evaporated and purified by flash chromatography (DCM/EtOAc gradient from 4:1 to 1:1) to give tert-butyl (3S)-3-{[5-chloro-2-(1H-tetrazol-1-yl)benzyl]carbamoyl}isoxazolidine-2-carboxylate (357 mg, 87%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119673B2
Source datasetuspto-grants-2012_02
ORD IDord-b4e73c52171e4651b39f74f4fc2f4cb8
Source noteuspto-grants-2012_02