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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901635Generated: November 1, 2026

Hydrochloric Acid → HCID 23368426, compound

https://huagongshe.com/reaction/1901635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantHCID 23368550HCID 23368550—
SolventMethanolHCID 887—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
ProductHCID 23368426HCID 23368426—

Reaction Steps

To a solution of 0.67 g of 3-(2-tert-butoxycarbonylamino-4-hydroxybutoxy)-5-chloro-1,2-benzoisoxazole in 6 ml of methylene chloride is added 0.30 g of chlorosulfonyl isocyanate at -30° C., and the temperature is gradually elevated to 0° C., after which 5 ml of water is added and they are stirred for 30 minutes. The solvent is removed by distillation under reduced pressure, water and ethyl acetate are added to the residue obtained, and after shaking, the organic layer is separated. The separated organic layer is washed with a saturated saline solution and dried over anhydrous magnesium sulfate, after which the solvent is removed by distillation under reduced pressure. The oily product obtained is dissolved in 8 ml of methanol, and thereto is added 1.5 ml of a 2-propanol solution (6.5M) of hydrogen chloride at room temperature, after which they are subjected to reaction at the same temperature for 18 hours. The crystals precipitated are collected by filtration, to obtain 0.29 g of colorless, crystalline 3-(2-amino-4-carbamoyloxybutoxy)-5-chloro-1,2-benzoisoxazole hydrochloride having a melting point of 213.5°-215.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578627
Source datasetuspto-grants-1996_11
ORD IDord-d3726f4ac56b4aea9df949f55dfaebd4
Source noteuspto-grants-1996_11