Potential neuroleptic agents. 4. Chemistry, behavioral pharmacology, and inhibition of [3H]spiperone binding of 3,5-disubstituted N-[(1-ethyl-2-pyrrolidinyl)methyl]-6-methoxysalicylamides

DOI: 10.1021/jm00151a010

Source and publish data:

Journal of Medicinal Chemistry p. 61 - 69 (1986)

Update date:2022-08-04

Topics:

Authors:

de Paulis

Kumar Kumar

Johansson

Raemsby Raemsby

Hall Hall

Saellemark

Angeby-Moeller

Ogren Ogren

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Article abstract of DOI:10.1021/jm00151a010

A series of 3,5-disubstituted N-[(1-ethyl-2-pyrrolidinyl)methyl]-6-methoxysalicylamides was synthesized, starting from the 2,6-dimethoxybenzoic acids, by boron tribromide demethylation of the corresponding 3,5-disubstituted 2,6-dimethoxybenzamides and sep

Full text of DOI:10.1021/jm00151a010

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