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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901623Generated: November 1, 2026

Water → HCID 23368484, compound

https://huagongshe.com/reaction/1901623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantHCID 23368400HCID 23368400—
SolventDichloromethaneHCID 6344—
ProductHCID 23368484HCID 23368484—

Reaction Steps

To a solution of 0.11 g of 3-(2-tert-butoxycarbonylamino-3-hydroxypropoxy)-5-(N-methyl-N-tert-butoxycarbonylamino)-1,2-benzoisoxazole in 5 ml of methylene chloride is added 0.10 g of chlorosulfonyl isocyanate at -45° to -40° C., and the temperature is elevated to 0° C., after which they are subjected to reaction at the same temperature for one hour. To the reaction mixture is added 10 ml of water and they are subjected to reaction at 20°-25° C. for one hour, after which the organic layer is separated. The separated organic layer is dried over anhydrous magnesium sulfate and the solvent is then removed by distillation under reduced pressure, to obtain 0.10 g of yellow, oily 3-(3-carbamoyloxy-2-tert-butoxycarbonylaminopropoxy)-5-(N-methyl-N-tert-butoxycarbonylamino)-1,2-benzoisoxazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578627
Source datasetuspto-grants-1996_11
ORD IDord-a755f03cd5ab4e3c877762ee8eaf0f57
Source noteuspto-grants-1996_11