Heterocyclyl carboxamides for treating viral diseases
Methods, uses, medicaments, and unit doses for treating viral diseases are described herein. The methods, uses, medicaments, and unit doses include (a) substituted piperidine and piperazine carboxamides, or a pharmaceutically acceptable salt thereof and (b) one or more pharmaceutically acceptable carriers, excipients or diluents, or combinations thereof. Viral diseases include hepatitis C virus, HIV, BVDV, and Coronavirus infections.
1. A method for treating an HCV or BVDV infection in a host animal, the method comprising the step of administering to the host animal a therapeutically effective amount of one or more compounds of the formula
or a pharmaceutically acceptable salt thereof; and wherein:
the one of more compounds each comprise a combination mode of Ar 1 , X, and R 2 , said combination mode selected from the group consisting of:
Com-
bina-
tion
Mode
Ar 1
X
R 2
1
3-(3-FC 6 H 4 )C 6 H 4
CH 2
Quinolin-8-yl
2
4-(3-MeC 6 H 4 )C 6 H 4
CH 2
4-OH-3-MeO—C 6 H 3
3
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2-OH-4-MeO—C 6 H 3
4
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
Quinolin-8-yl
5
4-(Benzimidazol-2-
CH 2
2-MeO—C 6 H 4
yl)C 6 H 4
6
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
4-OH-3,5-Me 2 —C 6 H 2
7
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
2-MeO—C 6 H 4
8
3-(3-FC 6 H 4 )C 6 H 4
CH 2
4-OH—C 6 H 4
9
3-(3-FC 6 H 4 )C 6 H 4
CH 2
2-(n-Bu)-imidazol-4-yl
10
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2,3-Methylenedioxy-C 6 H 3
11
3-(3-FC 6 H 4 )C 6 H 4
CH 2
3-OH—C 6 H 4
12
3-(3-FC 6 H 4 )C 6 H 4
CH 2
2-OH-6-MeO—C 6 H 3
13
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
4-OH—C 6 H 4
14
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
3-Me-4-MeO—C 6 H 3
15
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
3-MeO—C 6 H 4
16
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
4-F-2-MeO—C 6 H 3
17
3-(2-Indolyl)C 6 H 4
CH 2
(1-i-Pr-pyrazol-4-yl)
18
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
t-Bu
19
3-(2-Furyl)C 6 H 4
CH 2
Quinolin-8-yl
20
3-(2-Me-1,3,4-
C(═O)
2-Furyl
thiazol-5-yl)C 6 H 4
21
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
4-OH-3-MeO—C 6 H 3
22
3-indol-2-ylC 6 H 4
C(O)
C≡C—CH 3
23
4-benzimidazol-2-
CH 2
3-MeO—C 6 H 4
ylC 6 H 4
24
4-benzimidazol-2-
CH 2
5-Et-furan-2-yl
ylC 6 H 4
25
3-indol-2-ylC 6 H 4
C(O)
thiazol-5-yl
26
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
27
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
28
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
29
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
Et
30
4-benzimidazol-2-
CH 2
3-MeO—C 6 H 4
ylC 6 H 4
31
4-(3,5-Me 2 -pyrazol-
CH 2 CH═CH
2-MeO—C 6 H 4
1-yl)C 6 H 4
(E)
32
3-(3-FC 6 H 4 )C 6 H 4
CH 2
2-Et-5-Me-imidazol-4-yl
33
3-(3-MeOC 6 H 4 )C 6 H 4
CH 2
CH═C(Me) 2
34
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
3-MeO—C 6 H 4
35
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
naphtha-1-yl
36
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
1-allyl-3-Me-pyrazol-4-yl
37
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
1-Pr-5-Me-pyrazol-4-yl
38
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
Me
39
4-(2-FC 6 H 4 O)C 6 H 4
—
1-Et-piperidin-4-yl
40
3-(3-FC 6 H 4 )C 6 H 4
CH 2
1-(i-Pr)-3,5-Me 2 -pyrazol-4-yl
41
2-PhO-pyridin-5-yl
CH 2
Ph
42
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
1-Et-pyrazol-4-yl
43
3-(3-FC 6 H 4 )C 6 H 4
CH 2
3,5,6-Me 3 -pyrazin-2-yl
44
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
1-Pr-5-Me-pyrazol-4-yl
45
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2-HO-5-MeO—C 6 H 3
46
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
1-(i-Pr)-pyrazol-4-yl
47
2-PhO-pyridin-5-yl
CH 2
5-Cl-thien-2-yl
48
3-(3-FC 6 H 4 )C 6 H 4
CH 2
2,3-(MeO) 2 —C 6 H 3
49
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
4-HO-3-MeO—C 6 H 3
50
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
5-(i-Bu)-pyrazol-3-yl
51
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
3,5,6-Me 3 -pyrazin-2-yl
52
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
2,5-Me 2 —C 6 H 3
53
3-(3-FC 6 H 4 )C 6 H 4
CH 2
Benzo-2,1,3-thiadiazol-5-yl
54
3-(3-FC 6 H 4 )C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
55
4-(benzimidazol-2-
CH 2
Cyclohexen-4-yl
yl)C 6 H 4
56
3-(3-FC 6 H 4 )C 6 H 4
CH 2
1-allyl-3-Me-pyrazol-4-yl
57
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
5-Me-furan-2-yl
58
3-(3-FC 6 H 4 )C 6 H 4
CH 2
1-Et-5-Me-pyrazol-4-yl
59
4-(benzimidazol-2-
CH 2
3-FC 6 H 4
yl)C 6 H 4
60
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
1-Et-pyrazol-4-yl
61
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
Pyridin-2-yl
62
4-(Benzimidazol- 2-yl)Ph
—
63
3-(Indol-2-yl)Ph
—
64
4-(2-F—PhO)Ph
—
65
3-(3-F—Ph)Ph
—
66
3-Br—Ph
—
and one or more pharmaceutically acceptable carriers, excipients, or diluents, or combinations thereof.
2. The method of claim 1 , wherein the viral infection is a HCV infection.
3. The method of claim 1 , wherein the viral infection is a BVDV infection.
4. The method of claim 1 , wherein the one of more compounds each comprise a combination mode of Ar 1 , X, and R 2 , said combination mode selected from the group consisting of:
Com-
bina-
tion
Mode
Ar 1
X
R 2
1
3-(3-FC 6 H 4 )C 6 H 4
CH 2
Quinolin-8-yl
3
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2-OH-4-MeO—C 6 H 3
4
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
Quinolin-8-yl
5
4-(Benzimidazol-2-yl)C 6 H 4
CH 2
2-MeO—C 6 H 4
6
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
4-OH-3,5-Me 2 —C 6 H 2
7
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
2-MeO—C 6 H 4
8
3-(3-FC 6 H 4 )C 6 H 4
CH 2
4-OH—C 6 H 4
9
3-(3-FC 6 H 4 )C 6 H 4
CH 2
2-(n-Bu)-imidazol-4-yl
10
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2,3-Methylenedioxy-C 6 H 3
22
3-indol-2-ylC 6 H 4
C(O)
C≡C—CH 3
23
4-benzimidazol-2-ylC 6 H 4
CH 2
3-MeO—C 6 H 4
24
4-benzimidazol-2-ylC 6 H 4
CH 2
5-Et-furan-2-yl
26
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
27
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
28
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
29
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
Et
30
4-benzimidazol-2-ylC 6 H 4
CH 2
3-MeO—C 6 H 4
33
3-(3-MeOC 6 H 4 )C 6 H 4
CH 2
CH═C(Me) 2
38
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
Me
39
4-(2-FC 6 H 4 O)C 6 H 4
—
1-Et-piperidin-4-yl
40
3-(3-FC 6 H 4 )C 6 H 4
CH 2
1-(i-Pr)-3,5-Me 2 -pyrazol-4-yl
41
2-PhO-pyridin-5-yl
CH 2
Ph
42
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
1-Et-pyrazol-4-yl
43
3-(3-FC 6 H 4 )C 6 H 4
CH 2
3,5,6-Me 2 -pyrazin-2-yl
45
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2-HO-5-MeO—C 6 H 3
47
2-PhO-pyridin-5-yl
CH 2
5-Cl-thien-2-yl
49
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
4-HO-3-MeO—C 6 H 3
51
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
3,5,6-Me 3 -pyrazin-2-yl
54
3-(3-FC 6 H 4 )C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
56
3-(3-FC 6 H 4 )C 6 H 4
CH 2
1-allyl-3-Me-pyrazol-4-yl
58
3-(3-FC 6 H 4 )C 6 H 4
CH 2
1-Et-5-Me-pyrazol-4-yl
60
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
1-Et-pyrazol-4-yl
62
4-(Benzimidazol-2-yl)Ph
—
63
3-(Indol-2-yl)Ph
—
64
4-(2-F—PhO)Ph
—
65
3-(3-F—Ph)Ph
—
5. The method of claim 1 , wherein the one of more compounds each comprise a combination mode of Ar 1 , X, and R 2 , said combination mode selected from the group consisting of:
Combination
Mode
Ar 1
X
R 2
3
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2-OH-4-MeO—C 6 H 3
4
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
Quinolin-8-yl
5
4-(Benzimidazol-2-yl)C 6 H 4
CH 2
2-MeO—C 6 H 4
6
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
4-OH-3,5-Me 2 —C 6 H 2
39
4-(2-FC 6 H 4 O)C 6 H 4
—
1-Et-piperidin-4-yl
62
4-(Benzimidazol-2-yl)Ph
—
63
3-(Indol-2-yl)Ph
—
65
3-(3-F—Ph)Ph
—
6. The method of claim 2 , wherein the one of more compounds each comprise a combination mode of Ar 1 , X, and R 2 , said combination mode selected from the group consisting of:
Combination
Mode
Ar 1
X
R 2
1
3-(3-FC 6 H 4 )C 6 H 4
CH 2
Quinolin-8-yl
2
4-(3-MeC 6 H 4 )C 6 H 4
CH 2
4-OH-3-MeO—C 6 H 3
3
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2-OH-4-MeO—C 6 H 3
4
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
Quinolin-8-yl
5
4-(Benzimidazol-2-yl)C 6 H 4
CH 2
2-MeO—C 6 H 4
6
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
4-OH-3,5-Me 2 —C 6 H 2
7
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
2-MeO—C 6 H 4
8
3-(3-FC 6 H 4 )C 6 H 4
CH 2
4-OH—C 6 H 4
9
3-(3-FC 6 H 4 )C 6 H 4
CH 2
2-(n-Bu)-imidazol-4-yl
10
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2,3-Methylenedioxy-C 6 H 3
11
3-(3-FC 6 H 4 )C 6 H 4
CH 2
3-OH—C 6 H 4
12
3-(3-FC 6 H 4 )C 6 H 4
CH 2
2-OH-6-MeO—C 6 H 3
13
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
4-OH—C 6 H 4
14
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
3-Me-4-MeO—C 6 H 3
15
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
3-MeO—C 6 H 4
16
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
4-F-2-MeO—C 6 H 3
17
3-(2-Indolyl)C 6 H 4
CH 2
(1-i-Pr-pyrazol-4-yl)
18
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
t-Bu
19
3-(2-Furyl)C 6 H 4
CH 2
Quinolin-8-yl
20
3-(2-Me-1,3,4-thiazol-5-yl)C 6 H 4
C(═O)
2-Furyl
21
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
4-OH-3-MeO—C 6 H 3
22
3-indol-2-ylC 6 H 4
C(O)
C≡C—CH 3
23
4-benzimidazol-2-ylC 6 H 4
CH 2
3-MeO—C 6 H 4
24
4-benzimidazol-2-ylC 6 H 4
CH 2
5-Et-furan-2-yl
25
3-indol-2-ylC 6 H 4
C(O)
thiazol-5-yl
26
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
27
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
28
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
29
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
Et
30
4-benzimidazol-2-ylC 6 H 4
CH 2
3-MeO—C 6 H 4
31
4-(3,5-Me 2 -pyrazol-1-yl)C 6 H 4
CH 2 CH═CH(E)
2-MeO—C 6 H 4
32
3-(3-FC 6 H 4 )C 6 H 4
CH 2
2-Et-5-Me-imidazol-4-yl
33
3-(3-MeOC 6 H 4 )C 6 H 4
CH 2
CH═C(Me) 2
34
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
3-MeO—C 6 H 4
35
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
naphtha-1-yl
36
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
1-allyl-3-Me-pyrazol-4-yl
37
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
1-Pr-5-Me-pyrazol-4-yl
38
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
Me
39
4-(2-FC 6 H 4 O)C 6 H 4
—
1-Et-piperidin-4-yl
40
3-(3-FC 6 H 4 )C 6 H 4
CH 2
1-(i-Pr)-3,5-Me 2 -pyrazol-4-yl
41
2-PhO-pyridin-5-yl
CH 2
Ph
42
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
1-Et-pyrazol-4-yl
43
3-(3-FC 6 H 4 )C 6 H 4
CH 2
3,5,6-Me 3 -pyrazin-2-yl
44
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
1-Pr-5-Me-pyrazol-4-yl
45
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2-HO-5-MeO—C 6 H 3
46
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
1-(i-Pr)-pyrazol-4-yl
47
2-PhO-pyridin-5-yl
CH 2
5-Cl-thien-2-yl
48
3-(3-FC 6 H 4 )C 6 H 4
CH 2
2,3-(MeO) 2 —C 6 H 3
49
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
4-HO-3-MeO—C 6 H 3
50
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
5-(i-Bu)-pyrazol-3-yl
51
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
3,5,6-Me 3 -pyrazin-2-yl
52
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
2,5-Me 2 -C 6 H 3
53
3-(3-FC 6 H 4 )C 6 H 4
CH 2
Benzo-2,1,3-thiadiazol-5-yl
54
3-(3-FC 6 H 4 )C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
55
4-(benzimidazol-2-yl)C 6 H 4
CH 2
Cyclohexen-4-yl
56
3-(3-FC 6 H 4 )C 6 H 4
CH 2
1-allyl-3-Me-pyrazol-4-yl
57
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
5-Me-furan-2-yl
58
3-(3-FC 6 H 4 )C 6 H 4
CH 2
1-Et-5-Me-pyrazol-4-yl
59
4-(benzimidazol-2-yl)C 6 H 4
CH 2
3-FC 6 H 4
60
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
1-Et-pyrazol-4-yl
61
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
Pyridin-2-yl.
7. The method of claim 2 , wherein the one of more compounds each comprise a combination mode of Ar 1 , X, and R 2 , said combination mode selected from the group consisting of:
Combination
Mode
Ar 1
X
R 2
1
3-(3-FC 6 H 4 )C 6 H 4
CH 2
Quinolin-8-yl
3
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2-OH-4-MeO—C 6 H 3
4
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
Quinolin-8-yl
5
4-(Benzimidazol-2-yl)
CH 2
2-MeO—C 6 H 4
C 6 H 4
6
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
4-OH-3,5-Me 2 —C 6 H 2
7
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
2-MeO—C 6 H 4
8
3-(3-FC 6 H 4 )C 6 H 4
CH 2
4-OH—C 6 H 4
9
3-(3-FC 6 H 4 )C 6 H 4
CH 2
2-(n-Bu)-imidazol-4-yl
10
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2,3-Methylenedioxy-C 6 H 3
22
3-indol-2-ylC 6 H 4
C(O)
C≡C—CH 3
23
4-benzimidazol-2-ylC 6 H 4
CH 2
3-MeO—C 6 H 4
24
4-benzimidazol-2-ylC 6 H 4
CH 2
5-Et-furan-2-yl
26
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
27
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
28
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
29
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
Et
30
4-benzimidazol-2-ylC 6 H 4
CH 2
3-MeO—C 6 H 4
33
3-(3-MeOC 6 H 4 )C 6 H 4
CH 2
CH═C(Me) 2
38
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
Me
39
4-(2-FC 6 H 4 O)C 6 H 4
—
1-Et-piperidin-4-yl
40
3-(3-FC 6 H 4 )C 6 H 4
CH 2
1-(i-Pr)-3,5-Me 2 -pyrazol-
4-yl
41
2-PhO-pyridin-5-yl
CH 2
Ph
42
3-(3-ClC 6 H 4 )C 6 H 4
CH 2
1-Et-pyrazol-4-yl
43
3-(3-FC 6 H 4 )C 6 H 4
CH 2
3,5,6-Me 3 -pyrazin-2-yl
45
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2-HO-5-MeO—C 6 H 3
47
2-PhO-pyridin-5-yl
CH 2
5-Cl-thien-2-yl
49
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
4-HO-3-MeO—C 6 H 3
51
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
3,5,6-Me 3 -pyrazin-2-yl
54
3-(3-FC 6 H 4 )C 6 H 4
CH 2
2-HO-3-MeO—C 6 H 3
56
3-(3-FC 6 H 4 )C 6 H 4
CH 2
1-allyl-3-Me-pyrazol-4-yl
58
3-(3-FC 6 H 4 )C 6 H 4
CH 2
1-Et-5-Me-pyrazol-4-yl
60
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
1-Et-pyrazol-4-yl.
8. The method of claim 2 , wherein the one of more compounds each comprise a combination mode of Ar 1 , X, and R 2 , said combination mode selected from the group consisting of:
Combination
Mode
Ar 1
X
R 2
3
4-(2-FC 6 H 4 O)C 6 H 4
CH 2
2-OH-4-MeO—C 6 H 3
4
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
Quinolin-8-yl
5
4-(Benzimidazol-2-yl)C 6 H 4
CH 2
2-MeO—C 6 H 4
6
2-(3-MeOC 6 H 4 )C 6 H 4
CH 2
4-OH-3,5-Me 2 —C 6 H 2
39
4-(2-FC 6 H 4 O)C 6 H 4
—
1-Et-piperidin-4-yl.
9. The method of claim 3 , wherein the one of more compounds each comprise a combination mode of Ar 1 , X, and R 2 , said combination mode selected from the group consisting of:
Combination
Mode
Ar 1
X
R 2
22
3-indol-2-ylC 6 H 4
C(O)
C≡C—CH 3
23
4-benzimidazol-2-ylC 6 H 4
CH 2
3-MeO—C 6 H 4
24
4-benzimidazol-2-ylC 6 H 4
CH 2
5-Et-furan-2-yl
25
3-indol-2-ylC 6 H 4
C(O)
thiazol-5-yl
30
4-benzimidazol-2-ylC 6 H 4
CH 2
3-MeO—C 6 H 4
62
4-(Benzimidazol-2-yl)Ph
—
63
3-(Indol-2-yl)Ph
—
64
4-(2-F—PhO)Ph
—
65
3-(3-F—Ph)Ph
—
66
3-Br—Ph
—
10. The method of claim 3 , wherein the one of more compounds each comprise a combination mode of Ar 1 , X, and R 2 , said combination mode selected from the group consisting of:
Combination
Mode
Ar 1
X
R 2
22
3-indol-2-ylC 6 H 4
C(O)
C≡C—CH 3
23
4-benzimidazol-2-ylC 6 H 4
CH 2
3-MeO—C 6 H 4
24
4-benzimidazol-2-ylC 6 H 4
CH 2
5-Et-furan-2-yl
25
3-indol-2-ylC 6 H 4
C(O)
thiazol-5-yl
30
4-benzimidazol-2-ylC 6 H 4
CH 2
3-MeO—C 6 H 4
62
4-(Benzimidazol-2-yl)Ph
—
63
3-(Indol-2-yl)Ph
—
64
4-(2-F—PhO)Ph
—
65
3-(3-F—Ph)Ph
—
11. The method of claim 3 , wherein the one of more compounds each comprise a combination mode of Ar 1 , X, and R 2 , said combination mode selected from the group consisting of:
Combination
Mode
Ar 1
X
R 2
22
3-indol-2-ylC 6 H 4
C(O)
C≡C—CH 3
23
4-benzimidazol-2-ylC 6 H 4
CH 2
3-MeO—C 6 H 4
25
3-indol-2-ylC 6 H 4
C(O)
thiazol-5-yl
30
4-benzimidazol-2-ylC 6 H 4
CH 2
3-MeO—C 6 H 4
62
4-(Benzimidazol-2-yl)Ph
—
63
3-(Indol-2-yl)Ph
—
65
3-(3-F—Ph)Ph
—
12. A method for treating an HIV infection in a host animal, the method comprising the step of administering to the host animal a therapeutically effective amount of one or more compounds of the formula
or a pharmaceutically acceptable salt thereof; wherein the one of more compounds each comprise a combination mode of Ar 1 , X, and R 2 , said combination mode selected from the group consisting of:
Combination
Mode
Ar 1
X
R 2
22
3-indol-2-ylC 6 H 4
C(O)
C≡C—CH 3
23
4-benzimidazol-2-ylC 6 H 4
CH 2
3-MeO—C 6 H 4
24
4-benzimidazol-2-ylC 6 H 4
CH 2
5-Et-furan-2-yl
25
3-indol-2-ylC 6 H 4
C(O)
thiazol-5-yl
30
4-benzimidazol-2-ylC6H4
CH 2
3-MeO—C 6 H 4
and one or more pharmaceutically acceptable carriers, excipients, or diluents, or combinations thereof.
13. A method for treating a coronavirus infection in a host animal, the method comprising the step of administering to the host animal a therapeutically effective amount of one or more compounds selected from the group consisting of:
or a pharmaceutically acceptable salt thereof and one or more pharmaceutically acceptable carriers, excipients, or diluents, or combinations thereof.