Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409991Generated: October 26, 2026

Hexyl isocyanate → 1-Hexyl-3-(5-nitrobenzo[d]isothiazol-3-yl)urea

https://huagongshe.com/reaction/1409991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexyl isocyanateHCID 75659—
Reactant3-Amino-5-nitrobenzisothiazoleHCID 158638—
SolventTetrahydrofuranHCID 8028—
Product1-Hexyl-3-(5-nitrobenzo[d]isothiazol-3-yl)ureaHCID 12001420—

Reaction Conditions

Temperature70 °C

Reaction Steps

100 mg (0.513 mmol) of 5-nitrobenzo[d]isothiazol-3-ylamine were suspended in 5 ml of THF. Addition of 78.1 mg (0.61 mmol) of 1-isocyanatohexane was followed by stirring at RT for 2 h and at 70° C. for 2 h. Then a further 0.3 mmol of 1-isocyanatohexane was added, and stirring was continued at 70° C. for 6 h. The reaction mixture was concentrated, and the residue was dissolved in water and extracted with ethyl acetate. The organic phase was concentrated and purified by preparative HPLC (PR18, acetonitrile/water 0.1% TFA). Yield: 18 mg (11%), M+H+: 323.15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921404B2
Source datasetuspto-grants-2014_12
ORD IDord-1f78192f084d42d38cfcc2d2ac11c1be
Source noteuspto-grants-2014_12