HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-{[1-(5-chloro-1-methyl-1H-indol-2-yl)heptyl]amino}benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | methyl 4-{[1-(5-chloro-1-methyl-1H-indol-2-yl)heptyl]amino}benzoate | HCID 66778860 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-{[1-(5-chloro-1-methyl-1H-indol-2-yl)heptyl]amino}benzoic acid | HCID 66777812 | 98.1% |
Reaction Steps
To a mixture of methyl 4-{[1-(5-chloro-1-methyl-1H-indol-2-yl)heptyl]amino}benzoate (1.15 g) synthesized above, tetrahydrofuran (15 mL) and ethanol (15 mL) was added 1N is aqueous sodium hydroxide solution (15 mL), and the mixture was stirred overnight with heating under reflux, and concentrated under reduced pressure. The residue was dissolved in water (30 mL), and 1N hydrochloric acid (15 mL) was added at 0° C. The resulting precipitate was collected by filtration to give the title object compound (1.09 g, 98%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436043B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-a55f51df099949dda6fe05c4c2107db9 |
| Source note | uspto-grants-2013_05 |