IP Library Granted Patent US 8,772,502
Granted Patent B2
US 8,772,502 · App. 13/284,242 · Granted Jul 8, 2014

Alkylsulfinyl-substituted thiazolide compounds

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Quick Facts
Patent No.
US 8,772,502
App. No.
13/284,242
Granted
Jul 8, 2014
Kind
B2
Abstract

A new class of alkylsulfinyl thiazolides is described. These compounds show strong activity against hepatitis viruses.

Claims (50)

1. A compound of structural Formula (1):

and pharmaceutically acceptable salts thereof,

wherein R 1 is selected from the group consisting of hydrogen and Q-C(═O)—, any of which may be optionally substituted;

R 2 to R 5 are independently selected from the group consisting of hydrogen, D, hydroxy, F, Cl, Br, CN, NO 2 , (C 1 -C 6 )-alkyl, (C 3 -C 8 )-cycloalkyl, (C 1 -C 6 )-alkoxy, carboxy, (C 1 -C 6 )-alkoxycarbonyl, amino, (C 1 -C 6 )-acylamino, amido, (C 1 -C 6 )-alkylamido, (C 1 -C 6 )-dialkylamido, (C 1 -C 6 )-alkylsulfonylamino, (C 1 -C 6 )-haloalkyl, (C 1 -C 6 )-perhaloalkyl, (C 1 -C 6 )-perhaloalkoxy, (C 1 -C 6 )-alkyithio, (C 1 -C 6 )-alkylthioalkyl, (C 1 -C 6 )-alkylsulfonyl, (C 3 -C 8 )-cycloalkylsulfonyl, arylsulfonyl, arylalkylsulfonyl, heteroarylsulfonyl, heteroarylalkylsulfonyl, (C 1 -C 6 )-alkylsulfonamido, N,N′-(C 1 -C 6 )-dialkylsulfonamido, aryl, aryloxy, arylthio, arylalkylthio, heteroaryl, heteroaryloxy, heteroarylalkoxy, heteroarylthio, heteroarylalkylthio, heterocycloalkyl, heterocycloalkoxy, and Q-C(═O)— , any of which may be optionally substituted; or any two contiguous R 1 , R 2 or R 3 moieties may be combined together with the atoms to which they are attached and joined to form an optionally substituted 5-to 8-membered heterocycloalkyl ring;

wherein when one of R 6 or R 7 is hydrogen, the other is independently selected from the group consisting of (C 1 -C 6 )-alkylsulfinyl, (C 1 -C 6 )alkylsulfinyalkyl, (C 2 -C 6 )-alkenylsulfinyl, (C 2 -C 6 )-alkynylsulfinyl, (C 3 -C 8 )-cycloalkylsulfinyl, (C 5 -C 8 )-cycloalkenylsulfinyl, arylsulfinyl, arylalkylsulfinyl, arylalkenylsulfinyl, heteroarylsulfinyl, heteroarylalkylsulfinyl, heteroarylalkenylsulfinyl, and heterocycloalkylsulfinyl, any of which may be optionally substituted; or the R 6 and R 7 moieties may be combined together with the atoms to which they are attached and joined to form an optionally substituted 5-to 8-membered ring that incorporates a sulfinyl (—S[O]—) moiety; and

wherein Q is R 8 , OR 8 , NHR 8 , or NR 8 R 9 ; R 8 and R 9 are independently selected from the group consisting of hydrogen, (C 1 -C 12 )-alkyl, (C2-C 12 )-alkenyl, (C 2 -C 12 )-alkynyl, (C 3 -C 8 )-cycloalkyl, aryl, arylalkyl, arylalkenyl, heterocycloalkyl, heteroaryl, heteroarylalkyl, and heteroarylalkenyl, any of which may be optionally substituted; or R 8 and R 9 , together with the atoms to which they are attached, may be joined to form an optionally substituted 5-to 8-membered heterocycloalkyl ring; any of which may be optionally substituted.

2. The compound according to claim 1 ,

R 2 to R 5 are independently selected from the group consisting of hydrogen, D, hydroxy, F, Cl, Br, CN, NO 2 , (C 1 -C 6 )-alkyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 6 )-alkoxy, (C 1 -C 6 )-alkoxycarbonyl, (C 1 -C 6 )dialkylamido, (C 1 -C 3 )-haloalkyl, (C 1 -C 4 )-perhaloalkyl, (C 1 -C 4 )-perhaloalkoxy, (C 1 -C 6 )-alkylthio, (C 1 -C 6 )-alkylsulfonyl, (C 3 -C 6 )-cycloalkylsulfonyl, arylsulfonyl, arylalkylsulfonyl, heteroarylsulfonyl, heteroarylalkylsulfonyl, aryl, aryloxy, arylthio, heteroaryl, heteroaryloxy, heterocycloalkyl, and heterocycloalkoxy, any of which may be optionally substituted;

wherein when one of R 6 or R 7 is hydrogen, the other is independently selected from the group consisting of (C 1 -C 6 )-alkylsulfinyl, (C 1 -C 6 )-alkylsulfinylalkyl, (C 3 -C 8 )-cycloalkylsulfinyl, (C 5 -C 8 )-cycloalkenylsulfinyl, arylsulfinyl, arylalkylsulfinyl, heteroarylsulfinyl, heteroarylalkylsulfinyl, and heterocycloalkylsulfinyl, any of which may be optionally substituted; or the R 6 and R 7 moieties may be combined together with the atoms to which they are attached and joined to form an optionally substituted 5- to 7-membered ring that incorporates a sulfinyl (—S[O]—) moiety; and

wherein Q is R 8 , OR 8 , NHR 8 , or NR 8 R 9 ; R 8 and R 9 are independently selected from the group consisting of hydrogen, (C 1 -C 12 )-alkyl, (C 2 -C 12 )-alkenyl, (C 3 -C 8 )-cycloalkyl, aryl, arylalkyl, arylalkenyl, heterocycloalkyl, heteroaryl, heteroarylalkyl, and heteroarylalkenyl, any of which may be optionally substituted; or R 8 and R 9 , together with the atoms to which they are attached, may be joined to form an optionally substituted 5-to 7-membered heterocycloalkyl ring; any of which may be optionally substituted.

3. The compound according to claim 2 ,

wherein R 2 to R 5 are independently selected from the group consisting of hydrogen, D, F, Cl, Br, CN, (C 1 -C 6 )-alkyl (C 3 -C 6 )-cycloalkyl, (C 1 -C 6 )-alkoxy, (C 1 -C 3 )-haloalkyl, (C 1 -C 4 )-perhaloalkyl, (C 1 -C 4 )-perhaloalkoxy, (C 1 -C 6 )-alkyithio, aryl, aryloxy, heteroaryl, heteroaryloxy, heterocycloalkyl, and heterocycloalkoxy, any of which may be optionally substituted: and

wherein R 7 is hydrogen and R 6 is independently selected from the group consisting of (C 1 -C 6 )-alkylsulfinyl, (C 1 -C 6 )-alkylsulfinylalkyl, (C 3 -C 6 )-cycloalkylsulfinyl, arylsulfinyl, arylalkylsulfinyl, heteroarylsulfinyl, heteroarylalkylsulfinyl, and heterocycloalkylsulfinyl, any of which may be optionally substituted; or the R 6 and R 7 moieties may be combined together with the atoms to which they are attached and joined to form an optionally substituted 5- to 7-membered ring that incorporates a sulfinyl (—S[O]—) moiety.

4. The compound according to claim 3 ,

wherein R 2 to R 5 are independently selected from the group consisting of hydrogen, D, F. Cl, Br, CN, (C 1 -C 6 )-alkyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 6 )-alkoxy, (C 1 -C 3 )-haloalkyl, (C 1 -C 4 )-perhaloalkyl, (C 1 -C 4 )-perhaloalkoxy, and (C 1 -C 6 )-alkylthio, any of which may be optionally substituted.

5. The compound according to claim 4 ,

wherein R 1 is selected from the group consisting of hydrogen, and Q is selected from hydrogen, methyl, ethyl, n-propyl, isopropyl, n-butyl, 2-methyl-1-propyl, sec-butyl, tert-butyl, 2,3-dimethylbutan-2-yl, cyclohexyl, 2,6-dimethylcyclohexyl, 1-methylcyclohexyl, phenyl, 4-pyridyl, benzyl, 4-pyridylmethyl, phenylethyl, (S)-1-hydroxy-(phenylethyl), 2-pyrazinyl, phenyethenyl, (E)-2-(4-pyridazinyl)-1-ethenyl, (E)-4-(2-)-1H-imidazolyl-1-ethenyl, 3-acetoxyl-1-propyl, ethoxycarbonylethyl, methoxylcarbonylpropyl, N-methylaminocarbonylethyl, N-ethylaminocarbonylpropyl, 3-(N-ethylaminocarbonyl)-2,2-dimethyl-1-propyl, N-(morpholinoethyl)aminocarbonylethyl, 3-pyridylmethylaminocarbonylethyl, 4-pyridylmethylaminocarbonylethyl, 4-pyridylmethylaminocarbonylpropyl, carboxyethyl, carboxypropyl, 2-piperidinyl,3-piperidinyl, 4-piperidinyl, 2-piperazinyl, (S)-1-aminoethyl, (R)-1-aminoethyl, (S)-1-aminoisobutyl, 1-aminocyclopropyl, methoxy, ethoxy, isopropoxy, isobutoxy, neopentyloxy, cyclohexyloxy, 4-piperdinyloxy,3-acetoxy-2methyl-1-propoxy, tert-pentyloxy, 4-acetoxybenzyloxy, 3-(4-acetoxyphenyl)-2-propenyloxy, (E)-2-methyl-4-(2-oxo-2,3-dihydrobenzofuran-5-yl)but-3-en-2-yloxy, pivaloyloxymethoxy, pivaloyloxy-1-ethoxy, isopropoxycarbonyloxymethoxy, isopropoxycarbonyloxy-1-ethoxy, amino, N-methylamino, N-ethylamino N,N-dimethylamino, N-propylamino, N-isopropylamino, N-butylamino, N-piperidinyl, N-piperazinyl, N-4methylpiperazinyl, N-cyclohexylamino, N-benzylamino, N-(2,4-dimethoxy)benzylamino, 2-(N-methylcarboxamido)phenylamino, N-methyl-2-hydroxyethylamino, N 1 ,N 2 -dimethyl-1,2-ethanediamin-1yl, N 1 , N 2 -diethyl-1,2-ethanediamin-1-yl, N 1 ,N 2 -dimethyl-1,3-propanediamin-1-yl, and N 1 -methyl-N 2 -(2-morpholinoethyl)-1,2-ethanediamin-1-yl.

6. The compound according to claim 5 ,

wherein R 2 to R 5 are independently selected from the group consisting of hydrogen, D, F, Cl, CN, methyl, ethyl, n-propyl, isopropyl, n-hexyl, cyclopropyl, methoxy, ethoxy, isopropoxy, trifluoromethyl, tetrafluroethoxy, methylthio, and t-butylthio, any of which may be optionally substituted; and

wherein R 6 is selected from the group consisting of methylsulfinyl, ethylsulfinyl, isopropylsulfinyl, methylsulfinylmethyl, 2-(ethylsulfinyl)ethyl, t-butylsulfinylmethyl, cyclopropylsulfinyl, cyclopentylsulfinyl, phenylsulfinyl, benzylsulfinyl, phenethylsulfinyl, 2-pyridylsulfinyl, 2-pyrazinylsulfinyl, 4-thiazolylsulfinyl, 4-pyridylmethylsulfinyl, 3-thienylmethylsulfinyl, 4-piperidinylsulfinyl, tetrahydro-2H -pyranylsulfinyl, any of which may be optionally substituted.

7. The compound according to claim 6 ,

wherein R 1 is selected from the group consisting of hydrogen and R 8 and R 9 in Q-C(═O)— is selected from the group consisting of methyl, ethyl, ethoxy, isopropoxy, isobutoxy, phenyl, phenylethenyl, 4-piperidinyl, N-piperazinyl, N-(2,4-dimethoxy)benzylamino, 2-(N-methylcarboxamido)-phenylamino, N 1 , N 2 -dimethyl-1,2-ethanediamin-1-yl, N 1 ,N 2 -dimethyl-1,2-ethanediamin-1-yl, N 1 ,N 2 -dimethyl-1,3-propanediamin-1-yl, and N 1 -methyl-N 2 -(2-morpholinoethyl)-1,2-ethanediamin-1-yl;

wherein R 2 to R 5 are independently selected from the group consisting of hydrogen, F, Cl, methyl, ethyl, cyclopropyl, methoxy, ethoxy, trifluoromethyl and methylthio, any of which may be optionally substituted; and

wherein R 6 is selected from the group consisting of methylsulfinyl, ethylsulfinyl, isopropylsulfinyl, methylsulfinylmethyl, t-butylsulfinylmethyl, cyclopropylsulfinyl, and benzylsulfinyl.

8. The compound according to claim 7 ,

wherein R 1 is selected from the group consisting of hydrogen and Q-C(═O)— , where R 8 is methyl;

wherein R 2 through R 5 are hydrogen; and

wherein R 6 is methylsulfinyl.

9. The compound according to claim 2 ,

wherein to R 2 to R 5 are independently selected from the group consisting of hydrogen, D, F, Cl, Br, CN, (C 1 -C 6 )-alkyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 6 )-alkoxy, (C 1 -C 3 )-haloalkyl, (C 1 -C 4 )-perhaloalkyl, (C 1 -C 4 )-perhaloalkoxy, (C 1 -C 6 )-alkylthio, aryl, aryloxy, heteroaryl, heteroaryloxy, heterocycloalkyl, and heterocycloalkoxy, any of which may be optionally substituted; and

wherein R 6 is hydrogen and is independently selected from the group consisting of (C 1 -C 6 )alkysulfinyl, (C 1 -C 6 )-alkysulfinylalkyl, (C 3 - 6 )-cycloalkylsulfinyl, arylsulfinyl, arylalkylsulfinyl, heteroarylsulfinyl, heteroarylalkylsulfinyl, and heterocycloalkylsulfinyl, any of which may be optionally substituted; or the R 6 and R 7 moieties may be combined together with the atoms to which they are attached and joined to firm an optionally substituted 5- to 7-membered ring that incorporates a sultinyl (—S[O]—) moiety.

10. The compound according to claim 9 ,

wherein R 2 to R 5 are independently selected from the group consisting of hydrogen,D, F, Cl, Br, CN, (C 1 -C 6 )-alkyl, (C 3 -C 6 )cycloalkyl, (C 1 -C 6 )-alkoxy, (C 1 -C 3 )-haloalkyl, (C l -C 4 )-perhaloalkyl, (C 1 -C 4 )-perhaloalkoxy, and (C 1 -C 6 )-alkylthio, any of which may be optionally substituted.

11. The compound according to claim 10 ,

wherein R 1 is selected from the group consisting of hydrogen, and Q is selected from hydrogen, methyl, ethyl, n-propyl, isopropyl, n-butyl, 2-methyl-1 -propyl, sec-butyl, tert-butyl, 2,3-dimethylbutan-2-yl, cyclohexyl, 2,6-dimethylcyclohexyl, 1-methylcyclohexyl, phenyl, 4-pyridyl, benzyl, 4-pyridylmethyl, phenylethyl, (S)-1 -hydroxy-(phenylethyl), 2-pyrazinyl, phenylethenyl, (E)-2-(4-pyridazinyl)-1-ethenyl, (E)-4-(2-)-1 H imidazolyl-1-ethenyl, 3-acetoxyl-1-propyl, ethoxycarbonylethyl, methoxylcarbonylpropyl, N-methylaminocarbonylethyl, N-ethylaminocarbonylpropyl, 3-(N-ethylaminocarbonyl)-2,2-dimethyl-1-propyl, N-(morpholinoethyl)aminocarbonylethyl, 3-pyridylmethylaminocarbonylethyl, 4-pyridylmethylaminocarbonylethyl, 4-pyridylmethylarninocarbonylpropyl, carboxyethyl, carboxypropyl, 2-piperidinyl, 3-piperidinyl, 4-piperidinyl, 2-piperazinyl, (S)-1-aminoethyl, (R)-1-aminoethyl, (S)-1 -aminoisobutyl, 1-aminocyclopropyl, methoxy, ethoxy, isopropoxy, isobutoxy, neopentyloxy, cyclohexyloxy, 4-piperidinyloxy, 3-acetoxy-2-methyl-1-propoxy, tert-pentyloxy, 4-acetoxybenzyloxy, 3-(4-acetoxyphenyl)-2-propenyloxy, (E)-2-methyl-4-(2-oxo-2,3-dihydrobenzofuran-5-yl)but-3-en-2-yloxy, pivaloyloxymethoxy, pivaloyloxy-1-ethoxy, isopropoxycarbonyloxymethoxy, isopropoxycarbonyloxy-1-ethoxy, amino, N-methylamino, N-ethylamino, N,N-dimethylamino, N-propylamino, N-isopropylamino, N-butylamino, N-piperidinyl, N-piperazinyl, N-4-methylpiperazinyl, N-cyclohexylamino, N-benzylamino, N-(2,4-dimethoxy)benzylamino, 2-(N-methylcarboxamido)phenylamino, N-methyl-2-hydroxyethylamino, N 1 ,N 2 -dimethyl-1,2-ethanediamin-1-yl, N 1 ,N 2 diethyl-1 ,2-ethanediamin-1-yl, N 1 ,N 2 -dimethyl-1,3-propanediamin-1-yl, and N 1 -methyl-N 2 -(2-morpholinoethyl)-1,2-ethanediamin-1-yl.

12. The compound according to claim 11 ,

wherein R 2 to R 5 are independently selected from the group consisting of hydrogen, D, F, Cl, CN, methyl, ethyl, n-propyl, isopropyl, n-hexyl, cyclopropyl, merhoxy, ethoxy, isopropoxy, trifluoromethyl, tetrafluoroethoxy, methylthio, and t-butylthio, any of which may be optionally substituted; and

wherein R 7 is selected from the group consisting of methylsulfinyl, ethylsulfinyl, isopropylsulfinyl, methylsulfinylmethyl, 2-(ethylsulfinyl)ethyl, t-butylsulfinylmethyl, cyclopropylsulfinyl, cyclopentylsulfinyl, phenylsulfinyl, benzylsulfinyl, phenethylsulfinyl, 2-pyridylsulfinyl, 2-pyrazinylsulfinyl, 4-thiazolylsulfinyl, 4-pyridylmethylsulfinyl, 3-thienylmethylsulfinyl, 4-piperidinylsulfinyl, and tetrahydro-2H -pyranylsulfinyl, any of which may be optionally substituted.

13. The compound according claim 12 ,

wherein R 1 is selected from the group consisting of hydrogen and R 8 and R 9 in Q-C(═O )— is selected from the group consisting of methyl, ethyl, ethoxy, isopropoxy, isobutoxy, phenyl, phenylethenyl, 4-piperidinyl, N-piperazinyl, N-(2,4-dimethoxy)benzylamino, 2-(N-methylcarboxamido)-phenylamino, N 1 ,N 2 -dimethyl-1,2-ethanediamin-1-yl, N 1 ,N 2 -diethyl- ,1,2-ethanediamin-1-yl, N 1 ,N 2 -dimethyl-1,3-propanediamin-1-yl, and N 1 -methyl-N 2 -(2-morpholinoethyl)-1,2-ethanediamin-1-yl ;

wherein R 2 to R 5 are independently selected from the group consisting of hydrogen, F, Cl, methyl, ethyl, cyclopropyl, methoxy, ethoxy, trifluoromethyl and methylthio, any of which may be optionally substituted; and

wherein R 7 is selected from the group consisting of methylsulfinyl, ethylsulfinyl, isopropylsulfinyl, methylsulfinylmethyl, t-butylsulfinylmethyl, cyclopropylsulfinyl, and benzylsulfinyl.

14. The compound according to claim 13 ,

wherein R 1 is selected from the group consisting of hydrogen and Q-C(═O)— , where R 8 is methyl;

wherein R 2 through R 5 are hydrogen; and

wherein R 7 is methylsulfinyl.

15. A compound selected from the group consisting of:

16. A compound selected from the group consisting of:

17. The compound according to claim 1 ,

wherein the salt is selected from the group consisting of acetate, adipate, alginate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, citrate, camphorate, camphorsulfonate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, fumarate, glucoheptanoate, glycerophosphate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethane-sulfonate, lactate, malate, maleate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, oxalate, thiocyanate, tosylate, undecanoate, lithium, sodium, calcium, potassium, aluminum, ammonium, tetraethylammonium, methylammonium, dimethylammonium, N-methylmorpholinium and ethanolammonium.

Assignments (6)
SECURITY INTEREST Recorded Nov 16, 2019
From: ROMARK BIOSCIENCES S.À R.L. LLC; ROMARK LABORATORIES, L.C.
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 051030/0613 →
SECURITY INTEREST Recorded Jul 2, 2018
From: ROMARK BIOSCIENCES S.À R.L. LLC; ROMARK LABORATORIES, L.C.
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 046254/0524 →
SECURITY INTEREST Recorded Dec 22, 2017
From: ROMARK BIOSCIENCES S.À R.L. LLC; ROMARK LABORATORIES, L.C.
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 044472/0001 →
RELEASE OF SECURITY INTEREST Recorded Mar 6, 2015
From: U.S. BANK NATIONAL ASSOCIATION
To: ROMARK LABORATORIES, L.C.; ROMARK MANUFACTURING, LLC; LAPICOR, N.V.
Reel/Frame 035108/0474 →
SECURITY AGREEMENT Recorded Sep 4, 2013
From: ROMARK LABORATORIES, L.C.; ROMARK MANUFACTURING, LLC; LAPICOR, N.V.
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 031156/0923 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2012
From: SEMPLE, J. EDWARD; ROSSIGNOL, JEAN-FRANCOIS
To: ROMARK LABORATORIES, L.C.
Reel/Frame 027505/0508 →