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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804470Generated: November 1, 2026

1,2-Dichloroethane → HCID 67459994, compound

https://huagongshe.com/reaction/1804470

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 58504340HCID 58504340—
ReactantHCID 58537179HCID 58537179—
SolventAcetonitrileHCID 6342—
ProductHCID 67459994HCID 67459994—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 4-tert-butyl-5-phenylisoxazole-3-carboxylic acid (25 mg, 0.102 mmol), HOBt (28.1 mg, 0.183 mmol), and diisopropylethylamine (0.071 mL, 0.408 mmol) in acetonitrile (1 mL) was added EDC (45.9 mg, 0.240 mmol) and (Z)-tert-butyl 1-(4-(N′-hydroxycarbamimidoyl)benzyl)azetidine-3-carboxylate (Int.1, 31.1 mg, 0.102 mmol). The reaction mixture was stirred at 80° C. for 5 h. The reaction mixture was concentrated, and the residue was diluted with ethyl acetate (3 mL), washed with a saturated aqueous solution of sodium bicarbonate (1 mL), washed with water (1 mL), washed with brine (1 mL), and dried over anhydrous sodium sulfate. Concentration followed by purification by preparative HPLC afforded tert-butyl 1-(4-(5-(4-tert-butyl-5-phenylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)benzyl)-azetidine-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354398B2
Source datasetuspto-grants-2013_01
ORD IDord-3f06549365fd45bfbe96477bfcced35d
Source noteuspto-grants-2013_01