HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromo-2-methoxy-6-methylaniline → N-(4-Bromo-2-methoxy-6-methylphenyl)-4-chloro-7-(1-ethylpropyl)-1-methyl-1H-benzimidazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromo-2-methoxy-6-methylaniline | HCID 10680218 | — |
| Reactant | 2,4-Dichloro-7-(1-ethylpropyl)-1-methyl-1H-benzimidazole | HCID 67273025 | — |
| Catalyst | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Solvent | Water ethylacetate | HCID 22728543 | — |
| Product | N-(4-Bromo-2-methoxy-6-methylphenyl)-4-chloro-7-(1-ethylpropyl)-1-methyl-1H-benzimidazol-2-amine | HCID 11977538 | 49.1% |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
A mixture of 2,4-dichloro-7-(1-ethylpropyl)-1-methyl-1H-benzimidazole (140 mg, 0.52 mmol), 4-bromo-2-methoxy-6-methylaniline (335 mg, 1.55 mmol) and 1-methyl-2-pyrrolidone (5 drops) was stirred at 130° C. for 2 days under nitrogen atmosphere. The mixture was dissolved in ethyl acetate/water, extracted with ethyl acetate and washed with brine. The organic layer was dried over magnesium sulfate, and concentrated to give a brown oil. The oil was subjected to chromatography on a silica gel (n-hexane/ethyl acetate=10:1-1:1) and crystallized from iso-propanol to afford the title compound as colorless crystals (115 mg, 49%). mp. 218-220° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163935B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-3a233be1286149ef8ebda5b23d3989da |
| Source note | uspto-grants-2012_04 |