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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426010Generated: October 30, 2026

Hydrochloric Acid → HCID 66703740, compound

https://huagongshe.com/reaction/426010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66703774HCID 66703774—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 66703740HCID 6670374056.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106190B2
Source datasetuspto-grants-2012_01
ORD IDord-3f9d93f54ccd4c6f81cedf37b3710807
Source noteuspto-grants-2012_01