HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095838Generated: November 1, 2026
Water → 6-[(4-Methoxybenzyl)oxy]-3-methylimidazo[1,2-a]pyridin-2-amine
https://huagongshe.com/reaction/2095838
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-[5-[(4-methoxybenzyl)oxy]-2-{[(4-methylphenyl)sulfonyl]imino}pyridin-1(2H)-yl]propanamide | HCID 66969088 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-[(4-Methoxybenzyl)oxy]-3-methylimidazo[1,2-a]pyridin-2-amine | HCID 58158516 | 68% |
Reaction Steps
To a suspension of 2-[5-[(4-methoxybenzyl)oxy]-2-{[(4-methylphenyl)sulfonyl]imino}pyridin-1(2H)-yl]propanamide (2.6 g, 5.71 mmol) in tetrahydrofuran (25 mL) was added trifluoroacetic acid anhydride (2.35 mL, 17.1 mmol) at 0° C., and the mixture was stirred at room temperature for 1 hr. 8N Aqueous sodium hydroxide solution was added to the reaction mixture until it reached pH 12 to 13, and the mixture was stirred at 50° C. for 5 hr. Water and ethyl acetate were added to the reaction mixture, and the mixture was extracted 3 times with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and filtered. The solvent was evaporated under reduced pressure. The obtained residue was washed with ethyl acetate and collected by filtration to give the title compound (1.0 g, 68%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445509B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-9db161f3373b4f0595b9266791ed0a7e |
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| Source note | uspto-grants-2013_05 |
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