HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712690Generated: October 29, 2026
HCID 117667637, compound → HCID 117667667, compound
https://huagongshe.com/reaction/712690
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 117667637 | HCID 117667637 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117667667 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181272B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-4d679feaa7a445dfb08c8c14631697f9 |
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| Source note | uspto-grants-2015_11 |
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