Process for preparing antiviral compounds
OwnerShashank Shekhar, Thaddeus S. Franczyk +4inventors
InventorsShashank Shekhar, Thaddeus S. Franczyk, David M. Barnes, Travis B. Dunn, Anthony R. Haight, Vincent S. Chan
Life of this patent
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Abstract
This disclosure is directed to: (a) processes for preparing a compound and salts thereof that, inter alia, are useful for inhibiting hepatitis C virus (HCV); (b) intermediates useful for the preparation of the compound and salts; (c) pharmaceutical compositions comprising the compound or salts; and (d) methods of use of such compositions.
Claims23
A process for preparing N-(6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl)methanesulfonamide (compound (A)) or a salt thereof, wherein the process comprises:
- sulfonamidating compound (5) using a transition metal catalyst precursor and a ligand or a salt thereof:
- wherein R1a is selected from the group consisting of p-tolyl, phenyl, methyl, ethyl, trifluoromethyl, perfluorobutyl, perfluoropentyl, perfluorohexyl, perfluorooctyl and isomers and homologs thereof;
- wherein the ligand is a compound of formula (I)
- wherein
- Ar1 and Ar2 are each independently aryl or heteroaryl, and wherein Ar1 and Ar2 are each independently optionally substituted with one or more R1 and R2, respectively;
- R1and R2 are independently selected at each occurrence from the group consisting of hydrogen;
- amino;
- hydroxyl;
- cyano;
- halo;
- alkyl;
- alkenyl;
- alkynyl;
- haloalkyl;
- haloalkoxy;
- oxoalkyl;
- alkoxy;
- alkylamino;
- dialkylamino;
- cycloalkyl optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- cycloalkyloxy optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- 5- or 6-membered heteroaryl optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- phenyl optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- hydroxyalkyl;
- hydroxyalkoxy;
- alkoxyalkyl;
- aminoalkyl;
- N-alkylaminoalkyl;
- N,N-dialkylaminoalkyl;
- N,N,N-trialkylammoniumalkyl;
- L1-C(O)—OR1′, L1-P(O)—(OR1′)2, or L1-S(O)2—OR1′, wherein L1is a bond or alkylene, and R1′ is selected from the group consisting of hydrogen, alkyl and hydroxyalkyl;
- L2-O—C(O)—R2′, wherein L2 is a bond or alkylene, and R2′ is alkyl or hydroxyalkyl;
- L3-C(O)—NR3′R4′, wherein L3 is a bond or alkylene, and R3′ and R4′ are each independently selected from the group consisting of hydrogen, alkyl, and hydroxyalkyl;
- L4-NR5′—C(O)—R6′, wherein L4 is a bond or alkylene, R5′ is hydrogen or alkyl, and R6′ is alkyl or hydroxyalkyl;
- sulfamoyl;
- N-(alkyl)sulfamoyl;
- N,N-(dialkyl)sulfamoyl;
- sulfonamide;
- sulfate;
- alkylthio;
- thioalkyl;
- and a ring containing an alkylene or —O—(CH2)m—O— formed by the joining together of any two R1 or any two R2 or an R1 and an R2, wherein m is 1, 2, 3 or 4;
- X is a phosphine of formula (Ia):
- wherein ring A is a monocyclic heterocyclic ring, bicyclic heterocyclic ring, or tricyclic heterocyclic ring, and wherein ring A includes 0 to 9 ring atoms in addition to the phosphorus and 2 carbon ring atoms of formula (Ia), wherein said ring atoms are each independently selected from the group consisting of carbon, oxygen, nitrogen and sulfur;
- or
- X is a phosphine of formula (Ib):
- or
- X is a phosphine fused to Ar1 to give a compound of formula (Ic):
- wherein, ring B is a phosphorus heterocyclic ring with 0 to 5 ring atoms in addition to the phosphorous and carbon ring atoms of formula (I-c), wherein said ring atoms are each independently selected from the group consisting of carbon, oxygen, nitrogen and sulfur, and
- wherein the ring atoms of ring A and ring B are each independently optionally substituted with one or more substituents selected from the group consisting of alkenyl;
- alkoxy;
- alkoxyalkyl;
- alkyl;
- alkylamino;
- alkylthio;
- alkynyl;
- aminoalkyl;
- N-alkylaminoalkyl;
- N,N-dialkylaminoalkyl;
- N,N,N-trialkylammoniumalkyl;
- arylalkyl optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- cycloalkyl optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- dialkylamino;
- halo;
- haloalkyl;
- fluoroalkyl;
- C5-6 heteroaryl optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- heterocycloalkyl optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- hydroxy;
- hydroxyalkyl;
- oxo;
- an exocyclic double bond optionally substituted with alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heterocyclyl, or heteroaryl;
- a 3- to 7-membered spiro ring containing zero, one, or two heteroatoms;
- phenyl optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- L1-C(O)—OR1′, L1-P(O)—(OR1′)2, or L1-S(O)2—OR1′, wherein L1 is a bond or alkylene, and R1′ is selected from the group consisting of hydrogen, alkyl or hydroxyalkyl;
- L2-O—C(O)—R2′, wherein L2 is a bond or alkylene, and R2′ is alkyl or hydroxyalkyl;
- L3-C(O)—NR3′R4′, wherein L3 is a bond or alkylene, and R3′ and R4′ are each independently selected from the group consisting of hydrogen, alkyl, and hydroxyalkyl;
- L4-NR5′—C(O)—R6′, wherein L4 is a bond or alkylene, R5′ is hydrogen or alkyl, and R6′ is alkyl or hydroxyalkyl;
- and L7-NR8′—S(O)2—R9′, wherein L7 is a bond or alkylene, R8′ is hydrogen or alkyl, and R9′ is alkyl or hydroxyalkyl;
- RP is selected from the group consisting of alkyl, alkenyl, alkynyl, cycloalkyl, aryl, and heteroaryl, wherein RP is optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- or RP is a bridging group between the phosphorus and another B ring atom, wherein RP is selected from the group consisting of alkylene, alkenylene, alkynylene, and —(CR41R42—O)q—, wherein R41 and R42 are each independently hydrogen or alkyl, and wherein q is 1 or 2, and wherein RP is optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- as to R10, R11, R12, and R13,
- i. R10 or R11 together with R12 or R13 form a ring;
- or
- ii. R10 and R11 together with the carbon atom to which they are attached form a spirocyclic ring and/or R12 and R13 together with the carbon atom to which they are attached form a spirocyclic ring;
- or
- iii. one or more of R10, R11, R12 and R13 form a ring together with a ring substituent of ring A;
- or
- iv. at least one of substituents R10, R11, R12, and R13 do not form a ring, said substituents are each independently selected from the group consisting of hydrogen;
- alkyl;
- alkenyl;
- haloalkyl;
- alkynyl;
- oxoalkyl;
- cycloalkyl optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- heterocyclyl optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- C5-6 heteroaryl optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- phenyl optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- hydroxyalkyl;
- alkoxyalkyl;
- aminoalkyl;
- N-alkylaminoalkyl;
- N,N-dialkylaminoalkyl;
- N,N,N-trialkylammoniumalkyl;
- thioalkyl;
- L13-C(O)—OR14′, L13-P(O)—(OR14′)2, or L13-S(O)2—OR14′, wherein L13 is a bond or alkylene, and R14′ is selected from the group consisting of hydrogen, alkyl and hydroxyalkyl;
- L15-O—C(O)—R16′, wherein L15 is alkylene and R16′ is alkyl or hydroxyalkyl;
- L17-C(O)—NR18′R19′, wherein L17 is a bond or alkylene, and R18′ and R19′ are each independently selected from the group consisting of hydrogen, alkyl, and hydroxyalkyl;
- and L20-NR21′—C(O)—R22′, wherein L20 is alkylene, R21′ is hydrogen or alkyl, and R22′ is alkyl or hydroxyalkyl;
- and
- as to R14 and R15,
- R14 and R15 together with the carbon atom to which they are attached form a spirocyclic ring;
- or
- one or more of R14 and R15 form a ring together with a ring atom or ring substituent of ring B,
- wherein, if any of substituents R14 and R15 do not form a ring, said substituents are each independently selected from the group consisting of hydrogen;
- alkyl;
- alkenyl;
- haloalkyl;
- alkynyl;
- oxoalkyl;
- cycloalkyl optionally substituted with alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heterocyclyl, or heteroaryl;
- heterocyclyl optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- C5-6 heteroaryl optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- phenyl optionally substituted with alkyl, alkenyl, alkynyl, alkoxy, cyano, halo, haloalkyl or haloalkoxy;
- hydroxyalkyl;
- alkoxyalkyl;
- aminoalkyl;
- N-alkylaminoalkyl;
- N,N-dialkylaminoalkyl;
- N,N,N-trialkylammoniumalkyl;
- thioalkyl;
- L13-C(O)—OR14′, L13-P(O)—(OR14′)2, or L13-S(O)2—OR14′ wherein L13 is a bond or alkylene, and R14′ is selected from the group consisting of hydrogen, alkyl and hydroxyalkyl;
- L15-O—C(O)—R16′ wherein L15 is alkylene, and R16′ is alkyl or hydroxyalkyl;
- L17-C(O)—NR18′R19′, wherein L17 is a bond or alkylene and R18′ and R19′ are each independently selected from the group consisting of hydrogen, alkyl, and hydroxyalkyl;
- and L20-NR21′—C(O)—R22′, wherein L20 is alkylene, R21′ is hydrogen or alkyl, and R22′ is alkyl or hydroxyalkyl.
A process for preparing N-(6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl)methanesulfonamide (compound (A)) or a salt thereof, wherein the process comprises:
- sulfonamidating compound (5) using a transition metal catalyst precursor and a ligand:
- wherein R1a is selected from the group consisting of p-tolyl, phenyl, methyl, ethyl, trifluoromethyl, perfluorobutyl, perfluoropentyl, perfluorohexyl, perfluorooctyl and isomers and homologs thereof;
- and
- wherein the ligand is selected from the group consisting of di-tert-butyl(2′,4′,6′-triisopropyl-3,4,5,6-tetramethylbiphenyl-2-yl)phosphine;
- 2,2,7,7-tetramethyl-1-(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphepane;
- 2,2,7,7-tetramethyl-1-(2′,4′,6′-triisopropyl-3,4,5,6-tetramethylbiphenyl-2-yl)phosphepane;
- di-tert-butyl(2′,4′,6′-triisopropyl-3,6-dimethoxybiphenyl-2-yl) phosphine;
- 7,7,9,9-tetramethyl-8-(2′,4′,6′-triisopropyl-3,6-dimethoxybiphenyl-2-yl)-1,4-dioxa-8-phosphaspiro[4.5]decane;
- 8-(2-(2-methoxynaphthalen-1-yl)phenyl)-7,7,9,9-tetramethyl-1,4-dioxa-8-phosphaspiro[4.5]decane;
- 7,7,9,9-tetramethyl-8-(2′,4′,6′-triisopropylbiphenyl-2-yl)-1,4-dioxa-8-phosphaspiro[4.5]decane;
- 2,2,6,6-tetramethyl-1-(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphinane;
- 8,8,10,10-tetramethyl-9-(2′,4′,6′-triisopropylbiphenyl-2-yl)-1,5-dioxa-9-phosphaspiro[5.5]undecane;
- 2,2,6,6-tetramethyl-1-(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphinan-4-ol;
- 8-(2′,6′-diisopropoxybiphenyl-2-yl)-7,7,9,9-tetramethyl-1,4-dioxa-8-phosphaspiro[4.5]decane;
- 1,3,5,7-tetramethyl-8-(2′,4′,6′-triisopropylbiphenyl-2-yl)-2,4,6-trioxa-8-phosphatricyclo[3.3.1.13,7]decane;
- 8-(2′,6′-dimethoxybiphenyl-2-yl)-7,7,9,9-tetramethyl-1,4-dioxa-8-phosphaspiro[4.5]decane;
- 6-methoxy-N,N-dimethyl-2′-(7,7,9,9-tetramethyl-1,4-dioxa-8-phosphaspiro[4.5]decan-8-yl)biphenyl-2-amine;
- 8-(2′-methoxy-1,1′-binaphthyl-2-yl)-7,7,9,9-tetramethyl-1,4-dioxa-8-phosphaspiro[4.5]decane;
- 8-(1,1′-binaphthyl-2-yl)-7,7,9,9-tetramethyl-1,4-dioxa-8-phosphaspiro[4.5]decane;
- 7,7,9,9-tetramethyl-8-(2-(naphthalen-1-yl)phenyl)-1,4-dioxa-8-phosphaspiro[4.5]decane;
- and 7,7,9,9-tetramethyl-8-(2-(naphthalen-2-yl)phenyl)-1,4-dioxa-8-phosphaspiro[4.5]decane.
Dependencies are inferred from the claim text.