Preparation of sufentanil citrate and sufentanil base

Abstract

Provided herein are processes for forming sufentanil citrate from sufentanil base. One process comprises forming sufentanil citrate in the presence of a polar non-aqueous solvent. Other processes comprise forming sufentanil citrate in the presence of water.

What is claimed is: 
     
         1 . A process for preparing solid sufentanil citrate, the process comprising:
 (a) forming a first mixture of sufentanil citrate by heating a first portion of sufentanil base with a molar excess of citric acid in water, the first portion of sufentanil base comprising about 10% to about 20% of the total amount of sufentanil base;   (b) cooling the first mixture of sufentanil citrate;   (c) forming a second mixture of sufentanil citrate by heating a second portion of sufentanil base with an approximate molar equivalent of citric acid in water, the second portion of sufentanil base comprising about 80% to about 90% of the total amount of sufentanil base;   (d) adding the second mixture of sufentanil citrate, without cooling, to the first mixture of sufentanil citrate to form a combined mixture;   (e) cooling the combined mixture to form solid sufentanil citrate; and   (f) recovering the solid sufentanil citrate.   
     
     
         2 . The process of  claim 1 , wherein the molar excess of citric acid to sufentanil base at (a) is from about 2.5:1 to about 4.0:1. 
     
     
         3 . The process of  claim 1 , wherein the molar excess of citric acid to sufentanil base at (a) is about 2.8:1. 
     
     
         4 . The process of  claim 1 , wherein the heating at (a) is to a temperature from about 70° C. to about 85° C. 
     
     
         5 . The process of  claim 1 , wherein the cooling at (b) is to a temperature of about 23° C. or less. 
     
     
         6 . The process of  claim 5 , further comprising maintaining the temperature of the first mixture of sufentanil citrate until (d). 
     
     
         7 . The process of  claim 1 , wherein the approximate molar equivalent of citric acid to sufentanil base at (c) is from about 0.9:1 to about 1.1:1. 
     
     
         8 . The process of  claim 1 , wherein the approximate molar equivalent of citric acid to sufentanil base at (c) is about 1:1. 
     
     
         9 . The process of  claim 1 , wherein the heating at (c) is to a temperature from about 90° C. to about 100° C. 
     
     
         10 . The process of  claim 1 , wherein the adding at (d) occurs over an extended period of time such that the combined mixture maintains a temperature from about 10° C. to about 23° C. 
     
     
         11 . The process of  claim 10 , wherein the extended period of time is from about 0.5 hour to about 4 hours. 
     
     
         12 . The process of  claim 1 , wherein the cooling at (e) is to a temperature from about 0° C. to about 5° C. 
     
     
         13 . The process of  claim 1 , wherein the recovering at (f) comprises filtering. 
     
     
         14 . The process of  claim 1 , further comprising drying the solid sufentanil citrate. 
     
     
         15 . The process of  claim 1 , wherein the first portion of sufentanil base comprises about 15% of the total amount of sufentanil base, and the second portion of sufentanil base comprises about 85% of the total amount of sufentanil base. 
     
     
         16 . The process of  claim 1 , wherein prior to forming the first mixture of sufentanil citrate, a first solution of citric acid is formed by mixing from about 4 mL to about 6 mL of water per gram of citric acid. 
     
     
         17 . The process of  claim 1 , wherein prior to forming the second mixture of sufentanil citrate, a second solution of citric acid is formed by mixing from about 12 mL to about 20 mL of water per gram of citric acid. 
     
     
         18 . The process of  claim 1 , further comprising:
 (g) contacting the mixture remaining after recovery of solid sufentanil citrate with a proton acceptor to form a sufentanil base mixture;   (h) cooling the sufentanil base mixture to form solid sufentanil base; and   (i) recovering solid sufentanil base.   
     
     
         19 . The process of  claim 18 , further comprising contacting solid sufentanil base with a non-polar solvent to form crystalline sufentanil base. 
     
     
         20 . The process of  claim 18 , wherein the proton acceptor comprises a hydroxide and the non-polar solvent is an alkane.