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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexyl isocyanate | HCID 75659 | — |
| Reactant | 3-Amino-5-nitrobenzisothiazole | HCID 158638 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Hexyl-3-(5-nitrobenzo[d]isothiazol-3-yl)urea | HCID 12001420 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921404B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-1f78192f084d42d38cfcc2d2ac11c1be |
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| Source note | uspto-grants-2014_12 |
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