HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 68582514, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Bromo-1-methyl-5-nitro-1H-imidazole | HCID 12708672 | — |
| Reactant | HCID 68579996 | HCID 68579996 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 68582514 | HCID 68582514 | — |
Reaction Steps
TEA (0.26 ml, 1.86 mmol) was added to a mixture of 2-bromo-1-methyl-5-nitro-1H-imidazole (G. B. Barlin, J. Chem. Soc. B, 1967, 641; 126 mg, 0.61 mmol,) and 3,4-dichloro-5-methyl-N-piperidin-4-yl-1H-pyrrole-2-carboxamide hydrochloride (Intermediate 1), 191 mg, 0.61 mmol) in 1-methyl-2-pyrrolidinone (1.5 ml). Using a Smith Microwave Synthesizer, the mixture was subjected to single-mode microwave at 150° C. for 30 min. EtOAc was added and the solution was washed with water (2×). The organic phase was separated, dried over MgSO4, and concentrated under vacuum. The crude material was purified by chromatography on silica gel using 50% EtOAc/hexanes to give 158 mg of the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709503B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-1de7355ed5eb466ca99cc4ed02138f16 |
| Source note | uspto-grants-2010_05 |