HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-(4,6-Dimethoxypyrimidine-2-yl)-2-methyl-7-metoxymethylindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1-(4,6-Dimethoxypyrimidin-2-yl)propan-2-one | HCID 11264052 | — |
| Reactant | 2-Methoxymethylphenylhydrazine | HCID 12979365 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(4,6-Dimethoxypyrimidine-2-yl)-2-methyl-7-metoxymethylindole | HCID 11573215 | 46.2% |
Reaction Steps
Into a reactor were fed 6.2 g (31.6 m moles) of 1-(4,6-dimethoxypyrimidine-2-yl)-2-propanone, 4.8 g (31.5 m moles) of 2-methoxymethylphenylhydrazine, 4.76 g (34.9 m moles) of zinc chloride and 60 ml of toluene. Refluxing was made for 2 hours with heating. After the completion of the reaction, the reaction mixture was cooled to room temperature. Water and ethyl acetate were added and phase separation was made. The ethyl acetate layer was concentrated. The resulting crystals were washed with diisopropyl ether to obtain 4.57 g (14.6 m moles) of 3-(4,6-dimethoxypyrimidine-2-yl)-2-methyl-7-metoxymethylindole. Yield: 46%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07271263B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-addf75bc37514be49c805392e473df7f |
| Source note | uspto-grants-2007_09 |