HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376157Generated: October 31, 2026
Sodium hydride → 3-amino-1-[(2,2-dimethyl-1,3-dioxan-5-yl)methyl]-3,4-dihydroquinolin-2(1H)-one
https://huagongshe.com/reaction/1376157
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (2,2-Dimethyl-1,3-dioxan-5-yl)methyl methanesulfonate | HCID 10998661 | — |
| Reactant | 3-Amino-3,4-dihydroquinolin-2(1H)-one--hydrogen chloride (1/1) | HCID 13499428 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-amino-1-[(2,2-dimethyl-1,3-dioxan-5-yl)methyl]-3,4-dihydroquinolin-2(1H)-one | HCID 21906830 | 57.1% |
Reaction Steps
Sodium hydride (60% in oil, 1.60 g, 39.80 mmol) was added to 3-amino-3,4-dihydroquinolin-2(1H)-one hydrochloride (3.59 g, 18.09 mmol), in anhydrous DMF (50 mL) at 0° C. over a period of 10 min. The reaction was stirred for a further 30 min before addition of (2,2-dimethyl-1,3-dioxan-5-yl)methyl methanesulfonate [CAS registary number 131372-64-0] (4.05 g, 18.09 mmol) and the reaction has then heated to 60° C. for a period of 16 h. The reaction was then cooled and evaporated before addition of sat. aqueous NaHCO3 (200 mL) and EtOAc (500 mL). The organic layer was then dried (MgSO4), filtered and evaporated and the residue was purified by column chromatography (MeOH:DCM, 3:37) to afford the title compound (3.00 g, 57%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07169927B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-ed493a177eb04dc0859eda4ebdbf598d |
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| Source note | uspto-grants-2007_01 |
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