HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → N-(2-methylcyclohexyl)-3,5-dimethoxy-4-(2-propynyloxy)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methylcyclohexylamine | HCID 23432 | — |
| Reactant | 3,5-Dimethoxy-4-(2-propynyloxy)benzoyl chloride | HCID 57445669 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(2-methylcyclohexyl)-3,5-dimethoxy-4-(2-propynyloxy)benzamide | HCID 57701169 | 83.7% |
Reaction Steps
To a mixture of 15 ml of THF and 0.45 g of 3,5-dimethoxy-4-(2-propynyloxy)benzoyl chloride were added 0.24 g of 2-methylcyclohexylamine and 0.27 g of triethylamine in order at room temperature. The mixture obtained was stirred at room temperature for 4 hours. Then, ethyl acetate was added to the reaction mixture and the mixture was filtered through Celite. The filtrate was concentrated under reduced pressure. The residue obtained was washed with methyl tert-butyl ether and hexane to obtain 0.49 g of N-(2-methylcyclohexyl)-3,5-dimethoxy-4-(2-propynyloxy)benzamide (hereinafter, described as the compound 19 of the present invention) represented by the formula:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902400B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-b9f4cc769b7e4f7ea4346a039bf97167 |
| Source note | uspto-grants-2011_03 |