HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615533Generated: October 27, 2026
2-Amino-4-methoxy-6-methyl-1,3,5-triazine → N-2-biphenylylsulfonyl-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)urea
https://huagongshe.com/reaction/615533
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Amino-4-methoxy-6-methyl-1,3,5-triazine | HCID 15466 | — |
| Reactant | 2-Biphenylylsulfonylisocyanate | HCID 13103320 | — |
| Catalyst | Dabco | HCID 9237 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | N-2-biphenylylsulfonyl-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)urea | HCID 13103322 | 85% |
Reaction Steps
14.0 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine were suspended in 100 ml of dry acetonitrile, and then 0.1 g of 1,4-diazabicyclo[2,2,2]octane was added thereto. To this mixture was added dropwise a solution of 28.5 g of 2-biphenylylsulfonyl isocyanate in 30 ml of xylene over an hour. During this addition, the reaction was accompanied by slight heat generation, and therefore cooling was applied as necessary. After the addition, the reaction was continued at room temperature for 5 hours and then at 40° C. for 5 hours. After allowing the mixture to cool to room temperature, the precipitated colorless crystals were filtered, washed with ether and dried to obtain 33.9 g of N-2-biphenylylsulfonyl-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)urea; m.pt. 190°-193° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04500342 |
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| Source dataset | uspto-grants-1985_02 |
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| ORD ID | ord-32218f8688e7402bb6fe566c05e97666 |
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| Source note | uspto-grants-1985_02 |
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