HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylimidazole → HCID 21087642, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | HCID 18172722 | HCID 18172722 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21087642 | HCID 21087642 | 70% |
Reaction Steps
0.25 ml of N-methylimidazole (3.1 mmol) was introduced into a solution of N-(5-methanesulphonylamino-1-hydroxynaphthalen-2-yl)-2-chloroacetamide obtained above in the preceding step (1 g, 3 mmol) in 20 ml of tetrahydrofuran. The reaction medium was heated under reflux for 8 hours. The precipitate formed was drained, washed abundantly with dioxane and dried under vacuum to constant weight to give 0.86 g of 3-[(1-hydroxy-5-methanesulphonylaminonaphthalen-2-ylcarbamoyl)methyl]-1-methyl-3H-imidazol-1-ium chloride in the form of a brown powder melting at 198° C., with a yield of 70%. The cation mass spectroscopy analysis: m/z=375 of the product obtained was consistent with that of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06605124B1 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-dbd6cab27e044fde99fa4f78a5fe921e |
| Source note | uspto-grants-2003_08 |