HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Methyl 4-chloro-1-(3-chloro-2-methoxyphenyl)isoquinoline-7-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 136372360 | HCID 136372360 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 4-chloro-1-(3-chloro-2-methoxyphenyl)isoquinoline-7-carboxylate | HCID 67775230 | 83.3% |
Reaction Steps
A mixture of methyl 4-chloro-1-(3-chloro-2-hydroxyphenyl)isoquinoline-7-carboxylate (150 mg), potassium carbonate (119 mg), iodomethane (245 mg), and DMF (3 mL) was stirred at room temperature for one day. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried, and concentrated under reduced pressure. The resulting residue was purified under silica gel column chromatography (hexane/ethyl acetate) to obtain methyl 4-chloro-1-(3-chloro-2-methoxyphenyl)isoquinoline-7-carboxylate (130 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853242B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-7dcc0344a7e0435b95696ea1840f9b24 |
| Source note | uspto-grants-2014_10 |