HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559828Generated: October 26, 2026
2-Aminothiazole → 2-[([[(2-Phenoxyanilino)sulfonyl]amino]carbonyl)amino]thiazole
https://huagongshe.com/reaction/559828
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | Benzenamine, 2-phenoxy- | HCID 75899 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[([[(2-Phenoxyanilino)sulfonyl]amino]carbonyl)amino]thiazole | HCID 59732845 | 66.6% |
Reaction Steps
To a solution of chlorosulfonyl isocyanate (0.22 ml, 2.5 mmol) in tetrahydrofuran (25 ml) were added 2-phenoxyaniline (0.37 g, 2.0 mmol) and DIEA (0.89 ml, 5.0 mmol) at −78° C. The solution was stirred and slowly allowed to warmed up to 0° C. To this reaction mixture, was added 2-amino thiazole (0.20 g, 2.0 mmol) and continued stirring at room temperature for 3 h. The reaction mixture was concentrated under reduced pressure and the crude product was purified by column chromatography (ethylacetate:hexanes, from 50:50 to 90:10 as eluent system) to afford the title compound (0.52 g, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063081B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-2767f934212a479eb68a8f532e7dca4c |
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| Source note | uspto-grants-2011_11 |
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