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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744695Generated: October 31, 2026

Hydrochloric Acid → HCID 20094419, compound

https://huagongshe.com/reaction/744695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 19422064HCID 19422064—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 20094419HCID 20094419—

Reaction Steps

6-[(2,3-Dihydro-1,4-benzodioxin-2-yl)methylamino]-N-[4-(trifluoromethyl)phenyl]hexanamide monohydrochloride (201 mg), 37% aqueous formaldehyde (0.18 mL) and sodium cyanoborohydride (38 mg) were stirred in methanol (4.8 mL) for 96 hours at 20°-25° C. under nitrogen atmosphere. Saturated sodium bicarbonate (20 mL) was added to the reaction and extracted with dichloromethane (2×20 mL). The combined extracts were dried (Na2SO4) and concentrated vacuo. The resulting oil was chromatographed eluting with ethyl acetate and 10:90 ethanol:ethyl acetate to give a white solid (Rf of 0.52 in 10:90 ethanol:ethyl acetate) which was dissolved in ethanol and treated with 1.0M aqueous HCl (1 ml). The solution was concentrated in vacuo to give an oil which was dissolved in 70:30 ethyl acetate:hexane and concentrated. A hygroscopic white solid (151 mg) remained. CIMS (CH4): 437 (100%), 301 (40%). Exact Mass (CIMS, CH4): Calc. for C23H23F3N2O3 :437.2052. Found: 437.2044.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559143
Source datasetuspto-grants-1996_09
ORD IDord-bea9597cf60045f28a8cd176e1c098a7
Source noteuspto-grants-1996_09