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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 619478Generated: October 26, 2026

Formaldehyde → 4,5-Dihydro-4-(4-pentafluoropropionamidobutan-1-yl)-3H-1,4,8b-triazaacenaphthylene

https://huagongshe.com/reaction/619478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant5-[N-(4-pentafluoropropionamidobutan-1-yl)aminomethyl]imidazo[1,2-a]pyridineHCID 21190230—
SolventAcetic AcidHCID 176—
Product4,5-Dihydro-4-(4-pentafluoropropionamidobutan-1-yl)-3H-1,4,8b-triazaacenaphthyleneHCID 21190169—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2620 mg (7.19 mmol) of 5-[N-(4-pentafluoropropionamidobutan-1-yl)aminomethyl]imidazo[1,2-a]pyridine in 10 ml of acetic acid was added 8.1 ml (107.88 mmol) of a 37% aqueous solution of formalin. The mixture was heated for 30 minutes at 100° C. The solvent was distilled off under reduced pressure, and the residue was dissolved in 100 ml of purified water. To this solution was added 2N sodium hydroxide to adjust the pH to 8, and extracted with 100 ml of dichloromethane. The organic layer was washed with 100 ml of a saturated aqueous saline solution, dried over magnesium sulfate, and distilled off the solvent under reduced pressure. The residue was purified by silica gel column chromatography to afford 2250 mg of the desired compound (83.2%, a pale yellow liquid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05958942
Source datasetuspto-grants-1999_09
ORD IDord-88b60d0c9954474ebad0f568933ed0a8
Source noteuspto-grants-1999_09