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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765558Generated: November 4, 2026

Hydrochloric Acid → HCID 11269280, compound

https://huagongshe.com/reaction/1765558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantEther hydrochlorideHCID 10953452—
ReactantHCID 69497651HCID 69497651—
SolventEthyl AcetateHCID 8857—
ProductHCID 11269280HCID 11269280—

Reaction Steps

A solution of 3,4-dihydro-2H-pyrano[2,3-f]quinolin-3-amine (intermediate 1a) (0.20 g, 1.0 mmol), 3-(4-bromobutyl)-5-fluoro-1H-indole (0.19 g, 0.84 mmol), and triethylamine (0.28 mL, 1.68 mmol) in anhydrous dimethylsulfoxide (20 ml) was stirred at 100° C. for 14 hrs. The reaction mixture was poured into ice-H2O and extracted with methylene chloride. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under vacuum. Chromatography (5% MeOH/CH2Cl2) afforded 0.06 g (18%) of product as a light brown oil and unreacted starting material. It was converted to the HCl salt by dissolution in ethyl acetate and addition of 1M HCl/Et2O solution (2.4 eq) to generate N-[4-(5-fluoro-1H-indol-3-yl)butyl]-3,4-dihydro-2H-pyrano[2,3-f]quinolin-3-amine bis-hydrochloride salt as an off-white solid: mp 173° C./dec. MS ESI m/z 390 [M+H]+. Elemental Analysis for C24H24FN3O·2.00 HCl.3.00 H2O; Calculated: C, 55.82; H, 6.25; N, 8.14. Found: C, 55.57; H, 6.06; N, 7.76.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07227023B2
Source datasetuspto-grants-2007_06
ORD IDord-87f48d14cc7d432eb4f0da05996626a5
Source noteuspto-grants-2007_06