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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712690Generated: October 29, 2026

HCID 117667637, compound → HCID 117667667, compound

https://huagongshe.com/reaction/712690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 117667637HCID 117667637—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117667667HCID 117667667—

Reaction Steps

To a cooled (0° C.) suspension of 6-(5-acetyl-pyridin-3-yl)-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester (125 mg, 0.35 mmol) in THF (2 mL) is added a solution of isopropylmagnesium chloride in THF (1.3M, 816 μL, 1.1 mmol). The resultant mixture is stirred warming to room temperature for 1 h. The reaction is quenched with saturated aqueous ammonium chloride solution and is extracted with EtOAc. The combined organic extracts are washed with water and brine, dried (Na2SO4) and concentrated under reduced pressure. The residue is taken up in MeOH (3 mL) and 4N HCl in 1,4-dioxane (3 mL) is added. The reaction is stirred at room temperature for 16 h and is concentrated to provide 3-methyl-2-[5-(5,6,7,8-tetrahydro-[1,8]naphthyridin-3-yl)-pyridin-3-yl]-butan-2-ol (131 mg) as the dihydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181272B2
Source datasetuspto-grants-2015_11
ORD IDord-4d679feaa7a445dfb08c8c14631697f9
Source noteuspto-grants-2015_11