HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → N-(2,3-dihydro-benzo[b]furan-7-sulfonyl)-N'-(4-dimethylamino-6-methoxy-1,3,5-triazin-2-yl)-urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Diphenyl carbonate | HCID 7597 | — |
| Reactant | 2,3-Dihydro-1-benzofuran-7-sulfonamide | HCID 20209882 | — |
| Reactant | 1,8-diazabicyclo(5,4,0)undec-7-ene DBU | HCID 67393213 | — |
| Reactant | HCID 178493192 | HCID 178493192 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(2,3-dihydro-benzo[b]furan-7-sulfonyl)-N'-(4-dimethylamino-6-methoxy-1,3,5-triazin-2-yl)-urea | HCID 13884818 | — |
Reaction Steps
8,0 g of 2,3-dihydro-7-sulfamoyl-benzo[b]furan (0,04 mol) and 7,1 g of diphenyl carbonate (0,04 mol) and 150 ml of acetonitrile are stirred together. To this suspension are added dropwise at 0°-5° C. 7,1 g (0,05 mol) of 1,8-diazabicyclo(5,4,0)-undec-7-ene DBU and the resulting solution is left to stand for 15 hours at room temperature. These are then added dropwise 4,4 g (0,045 mol) of methanesulfonic acid at 0°-5° C. An addition of 6,8 g (0,04 mol) of 2-amino-4-dimethylamino-6-methoxy-triazine is subsequently made and the resulting suspension is refluxed for two hours and the resulting turbid hot solution is filtered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04656273 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-6ec1709cce1b42df98d4de645bc9352d |
| Source note | uspto-grants-1987_04 |