HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 66703740, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 66703774 | HCID 66703774 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 66703740 | HCID 66703740 | 56.3% |
Reaction Steps
At room temperature, 1 M hydrochloric acid (0.38 mL) was added to an ethanol (20 mL) solution of 2-{[(1S,2S)-2-(benzyloxy)cyclohexyl]amino}-N-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)-4-(trifluoromethyl)benzamide (140 mg), 10% palladium-carbon (240 mg) was added, followed by stirring for 1 day under an atmosphere of hydrogen. After neutralizing with a saturated sodium bicarbonate aqueous solution extracting with chloroform, the organic layer was concentrated under a reduced pressure. By purifying the residue by silica gel column chromatography (hexane:ethyl acetate, 1:0 to 1:1), 2-{[(1S,2S)-2-hydroxycyclohexyl]amino}-N-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)-4-(trifluoromethyl)benzamide (66 mg) was obtained as an amorphous.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106190B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-3f9d93f54ccd4c6f81cedf37b3710807 |
| Source note | uspto-grants-2012_01 |