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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430074Generated: October 26, 2026

Hydrochloric Acid → HCID 18353676, compound

https://huagongshe.com/reaction/430074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium AcetateHCID 517045—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-[3,3-Diethoxypropylamino]-4-methoxyquinolineHCID 18353658—
ReactantHCID 18353681HCID 18353681—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18353676HCID 1835367680.9%

Reaction Steps

2-[3,3-Diethoxypropylamino]-4-methoxyquinoline (0.046 g, 0.15 mmol) in THF (4 ml) was treated with 0.5M HCl (2 ml) for 10 min. The reaction mixture was evaporated to dryness and to the residue in methanol/HOAc (1 ml/0.018 ml) was added NaOAc (0.024 g, 0.3 mmol), 2-(3,4-dichlorophenyl)azetidine (0.03 g) and sodium cyanoborohydride (0.009 g, 0.15 mmol). After reaction for 40 min at 20° C., the reaction was evaporated to dryness under reduced pressure, and the residue partitioned between ethyl acetate and sat. sodium bicarbonate. The organic layer was dried, evaporated to dryness under reduced pressure and purified by chromatography on silica gel eluting with 1-3% (9:1 MeOH/NH3) in dichloromethane to give the title compound as a colourless gum (50 mg, 80%); δH (CD3OD) 1.55 (2H, m), 2.0 (1H, m), 2.25 (1H, m), 2.45-2.7 (2H, m), 2.8 (1H, m), 3.2-3.4 (4H, m), 3.9 (3H, s), 3.95 (1H, t), 6.0 (1H, s), 7.05 (1H, t), 7.15-7.5 (5H, m), 7.8 (1H, d); MS (ES+) 416/418 (47/32%, MH+), 244 (50), 201 (100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06320051B1
Source datasetuspto-grants-2001_11
ORD IDord-a3078d8c9b1840909e6517502c166810
Source noteuspto-grants-2001_11