HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 54516938, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 86738759 | HCID 86738759 | — |
| Reactant | HCID 178501943 | HCID 178501943 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54516938 | HCID 54516938 | — |
Reaction Steps
To a suspension of methyl 1-[[(4,6-dimethoxypyrimidin-2-yl)aminothiocarbonyl]aminosulfonyl]-2-naphthalenecarboxylate in 200 ml of anhydrous tetrahydrofuran can be added 16.7 ml of 3 M NaOCH3 /MeOH solution. The resulting reaction mixture can be heated to reflux, 3.1 ml of methyl iodide in 10 ml of anhydrous tetrahydrofuran can be added; and the reaction mixture can be refluxed for 3 hours. The reaction mixture can be cooled to cause the formation of a precipitate which can be filtered off and washed with tetrahydrofuran to afford the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04370479 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-568478ef52844844a098996a06538f15 |
| Source note | uspto-grants-1983_01 |