Pyrylium method of preparing pyrimidine cyclohexyl glucocorticoid receptor modulators
The present invention provides methods of preparing pyrimidine cyclohexyl glucocorticoid receptor modulators, methods of preparing intermediates of pyrimidine cyclohexyl glucocorticoid receptor modulators, and pyridinium compounds.
1 . A method of preparing a compound of Formula I:
the method comprising:
(a) forming a first reaction mixture comprising a first solvent, a strong acid, and a compound of Formula VII:
under conditions suitable to prepare the compound of Formula I,
wherein counterion X − is tetrafluoroborate, chloride, bromide, tetrachloroferrate, pentachlorostannate, hexafluorophosphate, butyltriphenylborate, or tetrakis(4-methoxyphenyl)borate.
2 . The method of claim 1 , wherein the first solvent comprises acetic acid, propionic acid, butyric acid, valeric acid, caproic acid, isobutyric acid, isovaleric acid, 4-methylvaleric acid, or 2-ethylcaproic acid.
3 . The method of claim 1 , wherein the strong acid comprises trifluoroacetic acid, trichloroacetic acid, ethane-1,2-disulfonic acid, naphthalene-2-sulfonic acid, naphthalene-1,5-disulfonic acid, hydrofluoric acid, hydrochloric acid, hydrobromic acid, hypochlorous acid, chloric acid, perchloric acid, sulfuric acid, nitric acid, phosphoric acid, methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, trifluoromethanesulfonic acid, camphorsulfonic acid, or combinations thereof.
4 . The method of claim 1 , wherein the strong acid comprises hydrochloric acid.
5 . The method of claim 1 , wherein counterion X − is BF 4 − .
6 . The method of claim 1 , wherein the compound of Formula VII has the structure:
7 . The method of claim 1 , comprising:
(a) forming the first reaction mixture comprising the compound of Formula VII, acetic acid, and concentrated hydrochloric acid, under conditions suitable to prepare the compound of Formula I.
8 . A method of preparing a compound of Formula VII:
comprising
(b) forming a second reaction mixture comprising a pyrylium salt:
a second solvent and a compound of Formula II, or a hydrate thereof:
under conditions suitable to prepare the compound of Formula VII, wherein counterion X − is BF 4 − .
9 . The method of claim 8 , wherein the pyrylium salt is pyrylium tetrafluoroborate having the structure:
10 . The method of claim 8 , wherein the pyrylium salt is present in an amount of from 1 to 3 molar equivalents to the compound of Formula II.
11 . The method of claim 8 , wherein the pyrylium salt is present in an amount of about 1.1 molar equivalents to the compound of Formula II.
12 . The method of claim 8 , wherein the second solvent comprises methanol, ethanol, n-propanol, isopropanol, n-butanol, t-butanol, 1-pentanol, 2-pentanol, 3-pentanol, 2-methyl-1-propanol, 1-methoxy-2-propanol, 4-methyl-2-pentanol, 1-hexanol, 2-hexanol, 1-octanol, or 2-octanol, or combinations thereof.
13 . The method of claim 8 , wherein the second solvent comprises n-propanol or n-butanol.
14 . The method of claim 8 , wherein the compound of Formula II is the monohydrate form:
15 . The method of claim 8 , comprising
(b) forming the second reaction mixture comprising pyrylium tetrafluoroborate in an amount of about 1.1 molar equivalents to the compound of Formula II, n-butanol, and the compound of Formula II, under conditions suitable to prepare the compound of Formula VII.
16 . The method of claim 1 , wherein the compound of Formula VII is prepared by
(b) forming a second reaction mixture comprising a pyrylium salt:
a second solvent and a compound of Formula II, or a hydrate thereof:
under conditions suitable to prepare the compound of Formula VII, wherein counterion X − is BF 4 − .
17 . The method of claim 16 , comprising:
(b) forming the second reaction mixture comprising pyrylium tetrafluoroborate in an amount of about 1.1 molar equivalents to the compound of Formula II, n-butanol, and the compound of Formula II, under conditions suitable to prepare the compound of Formula VII; and
(a) forming the first reaction mixture comprising the compound of Formula VII, acetic acid, and concentrated hydrochloric acid, under conditions suitable to prepare the compound of Formula I.
18 . A compound of Formula VII:
wherein counterion X − is tetrafluoroborate, chloride, bromide, tetrachloroferrate, pentachlorostannate, hexafluorophosphate, butyltriphenylborate, or tetrakis(4-methoxyphenyl)borate.
19 . The compound of claim 18 , wherein the compound of Formula VII has the structure: