HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxy-6-methylpyrimidin-2-amine → N-[(4-Methoxy-6-methyl-2-pyrimidinyl)aminocarbonyl]-4-nitrothiophene-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxy-6-methylpyrimidin-2-amine | HCID 587236 | — |
| Reactant | 4-Nitrothiophene-2-sulfonyl isocyanate | HCID 20215702 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-[(4-Methoxy-6-methyl-2-pyrimidinyl)aminocarbonyl]-4-nitrothiophene-2-sulfonamide | HCID 13203353 | — |
Reaction Steps
To 1.4 g of 2-amino-4-methoxy-6-methylpyrimidine in 25 ml of anhydrous acetonitrile was added 2.4 g of 4-nitrothiophene-2-sulfonyl isocyanate with stirring at ambient temperature. After stirring for sixteen hours, the mixture was filtered and the precipitate washed with 1-chlorobutane. It melted at 155° with decomposition and showed an infrared absorption spectrum with peaks at 1700, 1620 and 1570 cm-1 consistent for the desired structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04645529 |
| Source dataset | uspto-grants-1987_02 |
| ORD ID | ord-95052d81ca484487ac8271eb6afc828a |
| Source note | uspto-grants-1987_02 |