HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868999Generated: November 3, 2026
Ammonium Chloride → (3-Methylimidazo[2,1-f][1,6]naphthyridin-2-yl)methanol
https://huagongshe.com/reaction/868999
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Methyl 3-methylimidazo[2,1-f][1,6]naphthyridine-2-carboxylate | HCID 70115494 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3-Methylimidazo[2,1-f][1,6]naphthyridin-2-yl)methanol | HCID 70115904 | 50.5% |
Reaction Steps
A solution of methyl 3-methylimidazo[2,1-f][1,6]naphthyridine-2-carboxylate (100 mg, 0.39 mmol) in DCM (8 mL) was cooled to 0° C. Diisobutylaluminium hydride (1 M in cyclohexane, 1.2 mL, 1.2 mmol) was added dropwise over 10 min. Then the mixture was stirred at 0° C. for 1 h. 2 mL of saturated ammonium chloride aqueous solution was added slowly to quench the reaction. Then 5 mL of saturated sodium bicarbonate aqueous solution was added. The mixture was extracted with DCM (3×10 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated to give the crude product. The crude product was purified by column chromatography to give 42 mg of the product as a yellow solid. MS (ESI) m/z 214.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969349B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-308bca84d3d4470fa73d7a5ecc86d294 |
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| Source note | uspto-grants-2015_03 |
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