The invention relates to the technical field of
drug synthesis, in particular to a synthetic method of racemic 2, 6-dimethyl-2, 3-dihydro-1H-
indene-1-amine, N-acetyl-N-1-propenylacetamide and 2-fluoro-1, 4-dimethylbenzene are subjected to conjugation-like
addition reaction and
nucleophilic substitution reaction under the
catalysis of
copper reagents such as cuprous
iodide, and the racemic 2, 6-dimethyl-2, 3-dihydro-1H-
indene-1-amine is obtained through synthesis of racemic 2, 6-dimethyl-2, 3-dihydro-1H-
indene-1-amine and synthesis of racemic 2, 6-dimethyl-2, 3-dihydro-1H-indene-1-amine. The racemic 2, 6-dimethyl-2, 3-dihydro-1H-indene-1-amine is prepared by the following steps: introducing an amino group, and subsequently hydrolyzing under an alkaline condition, so that the racemic 2, 6-dimethyl-2, 3-dihydro-1H-indene-1-amine is conveniently obtained; the invention provides a more efficient,
safer and more economical solution for related synthesis reactions, has wide application prospects, provides a new idea and method for synthesis of the compounds, and improves the synthesis efficiency and quality of drugs.