HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235566Generated: October 30, 2026
Acetic Acid → 4-Dipropylamino-3-methyl-1,3-dihydroimidazo[4,5-c]pyridin-2-one
https://huagongshe.com/reaction/2235566
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Propanal | HCID 527 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 4-Amino-3-methyl-1,3-dihydro-2H-imidazo[4,5-c]pyridin-2-one | HCID 13516373 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 4-Dipropylamino-3-methyl-1,3-dihydroimidazo[4,5-c]pyridin-2-one | HCID 68584281 | — |
Reaction Steps
To a slurry of 750 mg (4.57 mmol) of 4-amino-3-methyl-1,3-dihydroimidazo[4,5-c]pyridin-2-one in 15 mL of dichloroethane was added 3.30 mL (45.7 mmol) of propionaldehyde, 1.0 mL of acetic acid, and 2.90 g (13.7 mmol) of sodium triacetoxyborohydride and the reaction was heated at 45° C. for 7.5 h. The reaction was diluted with 15 mL of dichloromethane and 15 mL of water and the aqueous layer was extracted with 15 mL of dichloromethane. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. The residue thus obtained (0.91 g, 80%) was used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07714009B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-cb882491b8b74f21b97e073eb064ba82 |
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| Source note | uspto-grants-2010_05 |
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