HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279735Generated: October 27, 2026
4-Methoxy-6-methylpyrimidin-2-amine → N-2-biphenylylsulfonyl-N'-(4-methoxy-6-methylpyrimidin-2-yl)urea
https://huagongshe.com/reaction/279735
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methoxy-6-methylpyrimidin-2-amine | HCID 587236 | — |
| Reactant | 2-Biphenylylsulfonylisocyanate | HCID 13103320 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-2-biphenylylsulfonyl-N'-(4-methoxy-6-methylpyrimidin-2-yl)urea | HCID 13103321 | 86.9% |
Reaction Steps
13.9 g of 2-amino-4-methoxy-6-methylpyrimidine were dissolved in 150 ml of dry dichloromethane. To this solution was added dropwise a solution of 28.5 g of 2-biphenylylsulfonyl isocyanate in 40 ml of toluene over an hour. During this addition, the internal temperature was maintained at room temperature. When the addition was finished, the mixture was stirred at room temperature for 10 hours to complete the reaction. After completion of the reaction, the mixture was concentrated to about half the volume by evaporating dichloromethane under reduced pressure. The resultant colorless crystals were filtered. The crystals were then washed with a small amount of ether and dried to obtain 34.6 g of N-2-biphenylylsulfonyl-N'-(4-methoxy-6-methylpyrimidin-2-yl) urea; m.p. 199°-202° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04586951 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-178020844ee249e4b3b0eaceec49e612 |
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| Source note | uspto-grants-1986_05 |
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