HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4,6-dimethyl pyrimidine → N-[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-2,3-dihydro-2,2-dimethyl-7-benzofuransulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4,6-dimethyl pyrimidine | HCID 13021 | — |
| Reactant | 2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-sulfonyl isocyanate | HCID 13424182 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-2,3-dihydro-2,2-dimethyl-7-benzofuransulfonamide | HCID 13424183 | 54.5% |
Reaction Steps
To a solution of 1.2 g of 2-amino-4,6-dimethylpyrimidine in 25 ml of tetrahydrofuran was added 2.5 g of 2,3-dihydro-2,2-dimethyl-7-benzofuransulfonyl isocyanate prepared above. After a slight exotherm the solution was stirred at room temperature for 4 hours. The solution was concentrated in vacuo to give a viscous oil that precipitated a solid from 10 ml of acetonitrile. The solid was recrystallized from acetonitrile to give 2 g of N-[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-2,3-dihydro-2,2-dimethyl-7-benzofuransulfonamide, m.p. 203°-206° C. The IR spectrum showed a carbonyl absorption at 1680 cm-1 indicative of a sulfonylurea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04514211 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-2c877a6f1c2846b8b78213b42efd28c5 |
| Source note | uspto-grants-1985_04 |