HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589134Generated: October 29, 2026
Isocyanatocarbonyl chloride → HCID 13506383, compound
https://huagongshe.com/reaction/1589134
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isocyanatocarbonyl chloride | HCID 119708 | — |
| Reactant | N-[4-(6-chlorobenzothiazol-2-ylthio)phenyl]-N'-methylurea | HCID 20236131 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 13506383 | HCID 13506383 | 77.6% |
Reaction Steps
Methyl isocyanate (0.41 g) was added to a solution of 4-(6-chlorobenzothiazol-2-ylthio)-aniline (2.0 g) in pyridine (20 ml), with stirring. The mixture was stirred at room temperature for 12 hours and evaporated to dryness. The residue was dissolved in a minimal volume of boiling ethanol and the solution was cooled in a refrigerator. The resulting solid substance was collected by filtration and dried to give N-[4-(6-chlorobenzothiazol-2-ylthio)phenyl]-N'-methylurea (1.5 g), which had a melting point of 289°-291° C. This urea (1.4 g) was dissolved in 1,4-dioxane (50 ml), and chlorocarbonyl isocyanate (0.47 g) was added. The mixture was heated at the boiling point for 5 hours and evaporated to dryness. The solid residue was dissolved in a minimal volume of boiling ethanol and the solution was cooled in a refrigerator. The resulting solid substance was collected by filtration and dried to give 1.3 g of 1-[4-(6-chlorobenzothiazol-2-ylthio)phenyl]-3-methyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione of melting point 232°-233° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04568674 |
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| Source dataset | uspto-grants-1986_02 |
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| ORD ID | ord-1cd8195710fe496f8ea2e51d2bf9d542 |
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| Source note | uspto-grants-1986_02 |
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