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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901608Generated: October 29, 2026

Ammonia → HCID 23368381, compound

https://huagongshe.com/reaction/1901608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
ReactantIsocyanatocarbonyl chlorideHCID 119708—
Reactant3-(2-Tert-butoxycarbonylamino-3-hydroxypropoxy)-5-chloro-1,2-benzoisoxazoleHCID 23368355—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 23368381HCID 23368381—

Reaction Steps

A solution of 1.00 g of 3-(2-tert-butoxycarbonylamino-3-hydroxypropoxy)-5-chloro-1,2-benzoisoxazole in 5 ml of methylene chloride is added to a solution of 0.31 g of N-(chlorocarbonyl) isocyanate in 10 ml of methylene chloride at -50° to -40° C. This solution is added to 10 ml of a methanol solution (8.0N) of ammonia at -20° C. over 20 minutes, and the temperature is elevated to 0° C., at which they are subjected to reaction for 30 minutes. Water is added to the reaction mixture, 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, to obtain 3-(3-ureidocarbonyloxy-2-tert-butoxycarbonylaminopropoxy)-5-chloro-1,2-benzoisoxazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578627
Source datasetuspto-grants-1996_11
ORD IDord-cf243cba3d204ff8bcb18a3ccb284af1
Source noteuspto-grants-1996_11