HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910248Generated: October 28, 2026
Dimethylformamide dimethyl acetal → HCID 67404651, compound
https://huagongshe.com/reaction/910248
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | 1-[4-(Imidazo[1,2-a]pyridin-2-yl)phenyl]ethan-1-one | HCID 21515561 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67404651 | HCID 67404651 | — |
Reaction Steps
Subsequently, N,N-dimethylformamide dimethyl acetal (3.0 mL) was added to a solution of 1-(4-imidazo[1,2-a]pyridin-2-ylphenyl)-1-ethanone (2.13 g) in N,N-dimethylformamide (50 mL), followed by heating at 120° C. for 8 hours. The reaction mixture was cooled to room temperature, and the precipitated solid was recovered through filtration, followed by washing with ethanol. The filtrate was concentrated under reduced pressure. The thus-obtained solid and the residue were subjected to flash chromatography. Fractions eluted by dichloromethane-methanol (30:1) were concentrated under reduced pressure, and the solid was recovered through filtration by use of ethyl acetate. Through the above procedure, (E)-3-dimethylamino-1-(4-imidazo[1,2-a]pyridin-2-ylphenyl)-2-propen-1-one (2.38 g) was yielded.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022075B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-3e0c21cf91ca4c4f982c4473d1c8fe1c |
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| Source note | uspto-grants-2011_09 |
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