HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598034Generated: October 30, 2026
Methane → 1-[7-bromo-2-(2-methoxyethyl)-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl]-2-methylpropan-2-ol
https://huagongshe.com/reaction/598034
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methane | HCID 297 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-{7-bromo-4-[(2-hydroxy-2-methylpropyl)amino][1,5]naphthyridin-3-yl}-3-methoxypropionamide hydrochloride | HCID 67052276 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | 1-[7-bromo-2-(2-methoxyethyl)-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl]-2-methylpropan-2-ol | HCID 67052530 | 73.6% |
Reaction Steps
A mixture of N-{7-bromo-4-[(2-hydroxy-2-methylpropyl)amino][1,5]naphthyridin-3-yl}-3-methoxypropionamide hydrochloride (60.00 g, 138 mmol), potassium carbonate (60 g), water (300 mL), and ethanol (900 mL) was heated at reflux for 16 hours and then concentrated under reduced pressure. The precipitated solid was isolated by filtration, washed sequentially with water and methanol, and dried to provide a brown solid. This material was dissolved in a 3/1 mixture of chloroform/methanol and decolorized with activated charcoal to provide 38.5 g of 1-[7-bromo-2-(2-methoxyethyl)-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl]-2-methylpropan-2-ol as a white solid, mp 125° C. Anal. calcd for C16H19BrN4O2: % C, 50.67; % H, 5.05; % N, 14.77; Found: % C, 50.86; % H 4.94; % N, 15.01.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897609B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-e8d15552fb994b4aa9f9580d693a6a65 |
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| Source note | uspto-grants-2011_03 |
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