Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763011Generated: October 27, 2026

9-amino-3,4-dihydroacridin-1(2H)-one → HCID 13756068, compound

https://huagongshe.com/reaction/1763011

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-amino-3,4-dihydroacridin-1(2H)-oneHCID 184361—
ReactantN,N,N',N'-TetramethylethanediamineHCID 17803068—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 13756068HCID 13756068—

Reaction Conditions

Temperature100 °C

Reaction Steps

In 25ml of trifluoroacetic acid cooled in ice was dissolved 5.00 g of 9-amino-3,4-dihydroacridin-1(2H)-one. To the solution was added dropwise 6.70ml (2.09 eq) of bisdimethylaminoethane over 5 minutes and thereafter the mixture was maintained at 90°100° C. for 5 hours during which the starting material was converted to a mixture of intermediate and exo-methylene products. The reaction mixture was poured into ice/NaOH to make it basic and the precipitate was extracted with several portions of 5:1 dichloromethane/MeOH. The combined extracts were evaporated to a residue. The residue was refluxed in toluene for 5 hours during which the intermediate was converted to the end product. The reaction mixture was evaporated to a residue which was purified by chromatography on silica gel (EtOAc) to yield about 2 g of a solid. This was recrystallized from dichloromethane/EtOAc to yield 1.79 g (34%) of product as a solid, melting point 119°-193° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04835275
Source datasetuspto-grants-1989_05
ORD IDord-5c49e10cd73648f487c86c6ac06105a2
Source noteuspto-grants-1989_05