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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547369Generated: October 31, 2026

1,4-Dioxane hydrochloride → HCID 59740849, compound

https://huagongshe.com/reaction/547369

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 59740842HCID 59740842—
SolventMethanolHCID 887—
ProductHCID 59740849HCID 5974084925%

Reaction Steps

tert-butyl (3-((6-cyclopentenyl-2-(3-fluorophenethylamino)nicotinamido)methyl)pyridin-2-yl)methylcarbamate was dissolved in MeOH (1 mL) and allowed to stir at room temperature. HCl/dioxane (4M, 2 mL) was added dropwise and stirred until complete. The reaction mixture was concentrated, diluted with EtOAc, washed with saturated sodium bicarbonate, brine and dried (Na2SO4). The organics were concentrated and purified by RP-HPLC with a mixture of acetonitrile and H2O to give N-((2-(aminomethyl)pyridin-3-yl)methyl)-6-cyclopentenyl-2-(3-fluorophenethylamino)nicotinamide as a solid (0.026 g, 25%). LC/MS (M+H+) m/z 446.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939534B2
Source datasetuspto-grants-2011_05
ORD IDord-1ff548f8b9634705bf7f9e7ada8cfb3e
Source noteuspto-grants-2011_05