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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944611Generated: November 1, 2026

Stannous chloride dihydrate → Methyl 1-(4-(3-amino-6-bromoquinolin-4-ylamino)-2-(trifluoromethyl)phenyl)piperidine-4-carboxylate

https://huagongshe.com/reaction/1944611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous chloride dihydrateHCID 61436—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 1-(4-(6-bromo-3-nitroquinolin-4-ylamino)-2-(trifluoromethyl)phenyl)piperidine-4-carboxylateHCID 67008148—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 1-(4-(3-amino-6-bromoquinolin-4-ylamino)-2-(trifluoromethyl)phenyl)piperidine-4-carboxylateHCID 6700834873.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of compound 8.2 methyl 1-(4-(6-bromo-3-nitroquinolin-4-ylamino)-2-(trifluoromethyl)phenyl)piperidine-4-carboxylate (0.26 g, 0.47 mmol, 1 equiv.) in dioxane (3 mL) at room temperature was added Tin(II) chloride dihydrate (0.53 g, 2.35 mmol, 5 equiv.). The resulting mixture was heated to 80° C. under argon for 5 hours. Upon cooling to room temperature, the mixture was neutralized with aqueous NaHCO3 and filtered. The filtrate was extracted with EtOAc (30 mL×2) and the combined organic layer was washed with water (50 mL) and brine (50 mL). The organic phase was dried over Na2SO4. After removal of solvent under vacuum, the resulting residue was purified via flash chromatography (hexanes:EtOAc 1:1) to afford desired product 8.3 methyl 1-(4-(3-amino-6-bromoquinolin-4-ylamino)-2-(trifluoromethyl)phenyl)piperidine-4-carboxylate (0.18 g; 73%). LC-MS (M+H): 523.10

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394818B2
Source datasetuspto-grants-2013_03
ORD IDord-af40d4c20060444683378719ac9860d3
Source noteuspto-grants-2013_03