Isoxazole carboxamide compounds
View Patent ↗The present disclosure provides substituted isoxazole carboxamide compounds having Formula (I) and the pharmaceutically acceptable salts and solvates thereof, wherein R 1 , R 2 , A, X, and Z are defined as set forth in the specification. The present disclosure is also directed to the use of compounds of Formula I to treat a disorder responsive to the blockade of SMYD proteins such as SMYD3 or SMYD2. Compounds of the present disclosure are especially useful for treating cancer.
1. A compound having Formula I:
or a pharmaceutically acceptable salt or hydrate thereof,
wherein:
R 1 is selected from the group consisting of C 1-6 alkyl, C 1-4 alkenyl, C 1-4 haloalkyl, C 3-6 cycloalkyl, and hydroxyalkyl;
R 2 is selected from the group consisting of hydrogen, halo, and carboxamido;
A is optionally substituted 4- to 14-membered heterocyclenyl;
with the provisos:
a) when R 1 is ethyl, n-propyl, isopropyl, isobutyl, or cyclopropyl; and R 2 is hydrogen, then A is not optionally substituted, optionally bridged piperidinenyl; and
b) when R 1 is C 1-6 alkyl or C 3-6 cycloalkyl; and R 2 is hydrogen, then A is not optionally substituted pyrrolidinenyl;
X is selected from the group consisting of —S(═O) 2 —, —S(═O) 2 N(R 7 )—, —N(R 7 )S(═O) 2 —, —S(═O) 2 C(R 8 )(H)—, —C(═O)—, —C(═O)N(R 7 )—, —N(R 7 )C(═O)—, —C(═O)O—, —OC(═O)—, —C(═O)C(R 8 )(H)N(R 7 )—, —N(R 7 )C(═O)C(R 8 )(H)—, —C(R 8 )(H)C(═O)N(R 7 )—, —C(R 8 )(H)N(R 7 )C(═O)—, and —C(═O)C(R 8 )(H)—; or X is absent;
Z is selected from the group consisting of hydrogen, optionally substituted C 1-6 alkyl, fluoroalkyl, hydroxyalkyl, amino, alkylamino, dialkylamino, heterocycloamino, (amino)alkyl, (alkylamino)alkyl, (dialkylamino)alkyl, (cycloalkylamino)alkyl, (heterocyclo)alkyl, (cycloalkyl)alkyl, (amino)(hydroxy)alkyl, (amino)(aryl)alkyl, (amino)(heteroaryl)alkyl (hydroxy)(aryl)alkyl, (aralkylamino)alkyl, (hydroxyalkylamino)alkyl, alkoxyalkyl, optionally substituted C 6-14 aryl, optionally substituted 4- to 14-membered heterocyclo, optionally substituted 5- to 14-membered heteroaryl optionally substituted C 3-12 cycloalkyl, aralkyl, and (heteroaryl)alkyl;
wherein —X—Z is attached to any available carbon or nitrogen atom of A;
R 7 is selected from the group consisting of hydrogen and C 1-4 alkyl; and
R 8 is selected from the group consisting of hydrogen, C 1-4 alkyl, hydroxy, amino, alkylamino, dialkylamino, cycloalkylamino, (amino)alkyl, (alkylamino)alkyl, (dialkylamino)alkyl, and hydroxyalkyl.
2. The compound of claim 1 , or a pharmaceutically acceptable salt or hydrate thereof, having Formula VI:
wherein:
R 11a and R 11b are each independently selected from the group consisting of hydrogen, C 1-4 alkyl, and alkoxycarbonyl;
X is selected from the group consisting of —C(═O)—, —S(═O) 2 —, and —C(═O)C(R 8 )(H)—;
Z is selected from the group consisting of (amino)alkyl, (alkylamino)alkyl, (dialkylamino)alkyl, (amino)(aryl)alkyl, (aralkylamino)alkyl, (heterocyclo)alkyl, optionally substituted C 3-12 cycloalkyl, and aralkyl; and
r is 0 or 1.
3. The compound of claim 1 , or a pharmaceutically acceptable salt or hydrate thereof, having Formula XVI:
wherein:
R 11c and R 11d are each independently selected from the group consisting of hydrogen and C 1-4 alkyl; and
X is selected from the group consisting of —C(═O)— and —S(═O) 2 ; or X is absent.
4. The compound of claim 3 , or a pharmaceutically acceptable salt or hydrate thereof, wherein:
R 11c and R 11d are hydrogen;
X is absent;
Z is selected from the group consisting of hydrogen, optionally substituted C 1-6 alkyl, fluoroalkyl, hydroxyalkyl, (amino)alkyl, (alkylamino)alkyl, (dialkylamino)alkyl, (heterocyclo)alkyl, (cycloalkyl)alkyl, (hydroxy)(aryl)alkyl, alkoxyalkyl, optionally substituted C 6-14 aryl, optionally substituted 4- to 14-membered heterocyclo, optionally substituted 5- to 14-membered heteroaryl, optionally substituted C 3-12 cycloalkyl, aralkyl, and (heteroaryl)alkyl; and
R 2 is hydrogen.
5. The compound of claim 1 , or a pharmaceutically acceptable salt or hydrate thereof, having Formula XVII:
wherein R″ is selected from the group consisting of aralkyl and (heteroaryl)alkyl.
6. The compound of claim 1 , or a pharmaceutically acceptable salt or hydrate thereof, wherein R 1 is selected from the group consisting of C 1-4 alkyl and C 3-6 cycloalkyl.
7. The compound of claim 6 , or a pharmaceutically acceptable salt or hydrate thereof, wherein R 1 is cyclopropyl.
8. The compound of claim 1 , or a pharmaceutically acceptable salt or hydrate thereof, selected from the group consisting of:
9. A pharmaceutical composition comprising the compound of claim 1 , or a pharmaceutically acceptable salt or hydrate thereof, and a pharmaceutically acceptable carrier.
10. A method of treating a patient comprising administering to the patient a therapeutically effective amount of the compound of claim 1 , or a pharmaceutically acceptable salt or hydrate thereof, wherein the patient has breast cancer, bladder cancer, cervical cancer, colon cancer, kidney cancer, liver cancer, lung cancer, head and neck cancer, skin cancer, pancreatic cancer, ovarian cancer, esophageal cancer, prostate cancer, or leukemia.