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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969580Generated: November 2, 2026

tert-Butyl ((1R,3S)-3-Isopropyl-3-{[3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl]carbonyl}cyclopentyl)carbamate → (1R,3S)-3-Isopropyl-3-{[3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl]carbonyl}cyclopentanamine

https://huagongshe.com/reaction/969580

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl ((1R,3S)-3-Isopropyl-3-{[3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl]carbonyl}cyclopentyl)carbamateHCID 60122330—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
Product(1R,3S)-3-Isopropyl-3-{[3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl]carbonyl}cyclopentanamineHCID 60122294117.2%

Reaction Steps

tert-Butyl ((1R,3S)-3-isopropyl-3-{[3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl]carbonyl}cyclopentyl)carbamate (300 mg, 0.6 mmol) was dissolved in a 4 M solution of HCl in 1,4-dioxane (20 mL). After being stirred at room temperature for 2 hrs, the solution was concentrated. The residue was treated with ether to give 250 mg of yellow solid. MS calculated for C18H24F3N3O: (M+H)+356; found 356.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07307086B2
Source datasetuspto-grants-2007_12
ORD IDord-5795720565de4b9291849d6591fb2044
Source noteuspto-grants-2007_12