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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978348Generated: October 29, 2026

Ammonium formate → HCID 20202901, compound

https://huagongshe.com/reaction/978348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantHCID 20202899HCID 20202899—
SolventWaterHCID 962—
ProductHCID 20202901HCID 202029015.2%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 1-(1-isoquinolyl)-3-(4-piperidyl)-1-propanone (2.5 g) and ammonium formate (7.5 g) is heated to 160° C. for 5 hours. The mixture is cooled, water (100 ml) is added, and the insoluble material is extracted with ethyl acetate (3×50 ml). After the solvent has been evaporated, the residue is taken up in 6N hydrochloric acid (35 ml) and boiled for 1 hour. The mixture is diluted with water (100 ml), the pH of the aqueous mixture is adjusted to 7, and the solution is extracted with ethyl acetate. The aqueous phase is made alkaline to pH 11, and extracted again with chloroform (3×100 ml). The organic phase is dried over magnesium sulphate and evaporated to dryness under reduced pressure. 1-(1-Isoquinolyl)-3-(4-piperidyl)-1-propanamine (0.13 g) is obtained, the proton NMR spectrum of which is deuterated chloroform has the following characteristics: ##STR8##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04665076
Source datasetuspto-grants-1987_05
ORD IDord-c3fc08a9669840d987a25570d4d16577
Source noteuspto-grants-1987_05