Process for preparation of pyrroles having hypolipidemic hypocholesteremic activities
The present invention provides pyrroles having hypolipidemic hypocholesteremic activities. The invention provides saroglitazar and its pharmaceutically acceptable salts, hydrates, solvates, polymorphs or intermediates thereof. The invention also provides a process for the preparation of saroglitazar. The invention further provides intermediates as well process for preparation thereof.
1. A process for the preparation of saroglitazar magnesium of Formula (I),
the process comprising:
(a) reacting a hydroxy compound (A) with a mesylate compound (A1) in a mixture of organic solvents comprising cyclohexane in the presence of a base and a phase transfer catalyst at a temperature between 35° C. and 85° C. to obtain an alkoxy ester compound of Formula (II);
(b) hydrolyzing the alkoxy ester compound of Formula (II) with a base to obtain saroglitazar; and
(c) reacting the saroglitazar with a magnesium source to obtain saroglitazar magnesium of Formula (I).
2. The process according to claim 1 , wherein the mixture of organic solvents further comprises one or more of alcohols selected from methanol, ethanol, isopropanol, 2 -propanol, 1 -butanol, and t-butyl alcohol; ketones selected from acetone, butarione, and methyl isobutyl ketone; esters selected from ethyl acetate, isopropyl acetate, t-butyl acetate, and isobutyl acetate; chlorinated hydrocarbons selected from methylene dichloride, ethylene dichloride, and chlorobenzene; hydrocarbons selected from pentane, hexane, and heptane; or ethers selected from tetrahydrofuran, 1 , 4 -dioxane, diisopropyl ether, diethyl ether, and methyl tert-butyl ether.
3. The process according to claim 1 , wherein in step (a), the base comprises one or more of sodium hydroxide, potassium hydroxide, lithium hydroxide, calcium hydroxide, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, sodium hydride, potassium hydride, potassium tert-butoxide, and sodium pentoxide.
4. The process according to claim 1 , wherein the phase transfer catalyst comprises one or more of tetrabutyl ammonium bromide (TBAB), tetrabutyl ammonium iodide (TBAI), benzyl triethyl ammonium chloride (TEBAC), a polyethylene Glycol, or a crown ether selected from the group consisting of 12-crown-4, 15-crown-5, 18-crown-6, dibenzo-18-crown-6, and diaza-18-crown-6.
5. The process according to claim 1 , wherein in step (b), the base comprises one or more of sodium hydroxide, potassium hydroxide, lithium hydroxide, calcium hydroxide, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, sodium hydride, and potassium hydride.
6. A process for the preparation of saroglitazar of Formula (IA), or a pharmaceutically acceptable salt thereof,
the process comprising:
(a) reacting a hydroxy compound (A) with a compound of Formula (A1′) in a mixture of organic solvents comprising cyclohexane in the presence of a base and a phase transfer catalyst at a temperature between 35° C. to 85° C. to obtain an alkoxy ester compound of Formula (II),
wherein, R is mesylate, tosylate, or triflate;
(b) hydrolyzing the alkoxy ester compound of Formula (II) with a base to obtain saroglitazar of formula (IA); and
(c) optionally, converting the saroglitazar to a pharmaceutically acceptable salt thereof.