Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273817Generated: November 1, 2026

Hydrochloric Acid → HCID 131717790, compound

https://huagongshe.com/reaction/273817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
Reactant2-Aminomethyl-1,4-benzodioxaneHCID 15053—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 15229344HCID 15229344—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 131717790HCID 13171779012.4%

Reaction Steps

2,3-Dihydro-1,4-benzodioxin-2-methanamine (350 mg) and 5-chloro-N-[4-(trifluoromethyl)phenyl]-pentanamide (593 mg) were stirred in dimethylformamide (7.0 mL) under a nitrogen atmosphere. Sodium bicarbonate (395 mg) and potassium iodide (40 mg) were added and mixture was stirred for 60 hours at 70°-75° C. Saturated sodium bicarbonate solution (50 mL) was added to the cooled reaction and the mixture extracted with diethyl ether (3×30 mL). The combined extracts were dried (MgSO4), filtered, and concentrated in vacuo. The resulting oil was chromatographed eluting with 40:60 ethyl acetate:hexane, then 10:90 ethanol:ethyl acetate to give a yellow-white solid with an Rf of 0.15 in 50:50 ethyl acetate:ethanol. This solid was dissolved in ethanol (20 mL) and treated with 1.0M aqueous HCl (1.0 mL). The solution was concentrated in vacuo to a white solid which after recrystallization from ethanol:ethyl acetate afforded the title compound as a white powder (117 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387604
Source datasetuspto-grants-1995_02
ORD IDord-6280104f02a1452983f96b57c34dbb91
Source noteuspto-grants-1995_02