HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 58980947, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 58980924 | HCID 58980924 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| Product | HCID 58980947 | HCID 58980947 | — |
Reaction Steps
A solution of 0.8 g (3.3 mmol) N-(tert-butyl)-5-formyl-1-methyl-1H-pyrrole-3-sulfonamide, 1.2 g (9.8 mmol) K2CO3 and 1 mL (16 mmol) CH3I in CH3CN was heated at 60° C. overnight. Solvent was removed, and the residue was partitioned between EtOAc and water. The organic layer was separated and washed with brine. Drying (MgSO4) and removal of solvent to give material that slowly solidified. The material was dissolved in 2 mL 1:1 CH2Cl2-TFA with stirring for 3 h. Solvent was removed to give the title compound as a solid, 1H NMR (DMSO) δ 9.8 (s, 1H), 7.9 (s, 1H), 7.45 (s, 1H), 7.4 (s, 1H), 4.1 (s, 3H), 2.6 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07285558B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-bb07b36f38b44cadba73c36b5182ade9 |
| Source note | uspto-grants-2007_10 |