Bromopride is a dopamine D2 receptor antagonist (Ki = 14 nM). It binds to bovine anterior pituitary membranes with an IC50 value of 2.13 μM. Bromopride inhibits cholinesterase activity in vitro in rat plasma and striatum homogenate (IC50s = 67.8 and 38.4 μM, respectively). It increases serum prolactin levels in rats by 100% when used at a dose of 0.02 mol/kg. Bromopride (2.5 mg/kg) decreases locomotion and rearing in an open field test and impairs acquistion, but not retention, of a conditioned avoidance response in a two-way active conditioned avoidance test in rats.
Praiden,Italchemi,Italy,1977
An antiemetic.Bromopride is used in method and a system for analyzing neuropharmacology of a drug.
ChEBI: 4-amino-5-bromo-N-[2-(diethylamino)ethyl]-2-methoxybenzamide is a member of benzamides.
To 119 g (0.45 mol) of N-(2-diethylaminoethyl)-2-methoxy-4-aminobenzamide
dissolved in 200 cc of acetic acid are added in the cold in small portions 69 g
of acetic anhydride (0.45 mol + 50% excess). The starting material is made
by esterifying 4-aminosalicylic acid with methanol, then acetylating with acetic
anhydride and then methylating with dimethyl sulfate. The solution obtained is
heated for 2 hours on a water bath and then boiled for 15 minutes. It is
cooled at 25°C. While agitating constantly and maintaining the temperature
between 25° and 30°C, there is added to the solution drop by drop 72 g of
bromine dissolved in 60 cc of acetic acid. It is agitated for one hour. The mixture obtained is added to one liter of water and the base is precipitated by
the addition of 30% soda, The precipitated base is extracted with 40 cc of
methylene chloride. After evaporation of the solvent, the residue is boiled for
two hours with 390 g of concentrated hydrochloric acid in 780 cc of water. It
is cooled, diluted with one liter of water, 12 g of charcoal are added, and the
mixture filtered. The base is precipitated with 30% soda. The N-(2-
diethylaminoethyl)-2-methoxy-4-amino-5-bromobenzamide formed
crystallizes, is centrifuged and washed with water. A yield of 85 g of base
having a melting point of 129°-130°C is obtained.
To produce the dihydrochloride, the free base is dissolved in 110 cc of
absolute alcohol, 9.6 g of dry hydrochloric acid dissolved in 35 cc of alcohol
are added, followed by 2.8 cc of water. The dihydrochloride precipitates, is
centrifuged, washed, and dried at 40°C. It was a solid white material having a
melting point of 134°-135°C.
