IMPROVED CHLORANTRANILIPROLE PROCESS THROUGH USE OF A CRYSTAL INTERMEDIATE
Disclosed are three-component crystals comprising compounds of Formula II, compounds of Formula III and an amine base in an equimolar ratio (1:1:1). Also disclosed are methods for preparing the three-component crystals comprising compounds of Formula II, compounds of Formula III and an amine base in an equimolar ratio (1:1:1). Further disclosed are methods for the preparation of chlorantraniliprole using the three-component crystals of the disclosure.
1 . A three-component crystal comprising
(a) a compound of Formula II:
(b) a compound of Formula III; and
(c) an amine base,
wherein the components are in an approximately equimolar ratio of 1:1:1.
2 . The three-component crystal of claim 1 , wherein the amine is a pyridine base.
3 . The three-component crystal of claim 1 , wherein the pyridine base is 3-picoline.
4 . The three-component crystal of claim 1 , having unit cell dimensions of about 12.12 Å×about 15.80 Å×about 12.28 Å.
5 . A method for the preparation of a three-component crystal comprising
(a) a compound of Formula II:
(b) a compound of Formula III; and
(c) an amine base,
the method comprising the steps of:
(i) forming an admixture of the compound of Formula II, the compound of Formula III and the amine base in an approximately equimolar amount of 1:1:1 in an aprotic solvent,
(ii) forming the three-component crystals therefrom, and
(iii) isolating the three-component crystals from the polar aprotic solvent.
6 . The method of claim 5 , wherein the aprotic solvent is acetonitrile.
7 . The method of claim 5 , wherein the amine base is a pyridine base.
8 . (canceled)
9 . A method for the preparation of a compound of Formula I
the method comprising the steps of:
(a) reacting a suspension of a three-component crystal comprising
(i) a compound of Formula II:
(ii) a compound of Formula III; and
(iii) an amine base,
in an aprotic solvent with an acid activating agent, wherein the components are present in an approximately equimolar ratio of 1:1:1, and
(b) allowing the coupling of acid activated compounds of Formulas II and III to proceed to the formation of the compound of Formula I.
10 . The method of claim 9 , wherein the aprotic solvent is acetonitrile.
11 . The method of claim 9 , wherein the acid activating agent is a sulfonyl chloride.
12 . (canceled)
13 . The method of claim 9 , wherein the amine base is a pyridine base.
14 . (canceled)
15 . A method for the preparation of a compound of Formula I
the method comprising the steps of:
(a) preparing a mixture comprising a compound of Formula II:
a compound of Formula III;
an amine base;
and an aprotic solvent,
(b) combining the mixture with an acid activating agent; and
(c) allowing the coupling of acid activated compounds of Formulas II and III to proceed to the formation of the compound of Formula I,
the method further comprising adding compound Formula I seed crystals, wherein the seed crystals are
(i) added when preparing the mixture of step (a),
(ii) added to the mixture before the acid activating agent has been added to the mixture in step (b), or
(iii) added during addition of the activating agent in step (b).
16 . The method of claim 15 , wherein the amount of seeding material of the compound of Formula I is in the range of about 0.5 mol-% to 15 mol-%.
17 . The method of claim 15 , wherein the mixture comprising the seeding material has a temperature in the range of from about 30° C. to reflux.
18 . (canceled)