IP Library Granted Patent US 9,657,030
Granted Patent B2
US 9,657,030 · App. 14/827,085 · Granted May 23, 2017

Transition metal-catalyzed processes for the preparation of N-allyl compounds and use thereof

Inventors: Joshua Robert Giguere (Sharon, MA); Keith Edward McCarthy (Old Lyme, CT); Helge Alfred Reisch (Westerly, RI); Sergio Sandoval (West Warwick, RI); Jake Larry Stymiest (Foster, RI)
Assignee: Rhodes Technologies
C07D489/08B01J23/42B01J23/44B01J31/1855B01J31/20B01J31/2295B01J31/2414C07C209/00C07C209/44C07C269/04C07D265/30C07D295/03C07D295/205B01J2231/40B01J2531/64B01J2531/821B01J2531/824B01J2531/828B01J2531/847Y02P20/55
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Quick Facts
Patent No.
US 9,657,030
App. No.
14/827,085
Granted
May 23, 2017
Kind
B2
Abstract

The present disclosure provides processes for the N-dealkylation of tertiary amines and the use of transition metal catalysts to prepare tertiary N-allyl amine derivatives and secondary amine derivatives thereof. The tertiary amines can be alkaloids and, more particularly, the tertiary amines can be opioids. In specific embodiments, the present disclosure provides methods for use in processes for the synthesis of naloxone and naltrexone from oripavine.

Claims (42)

1. A method for making a compound of Formula (54)

comprising

contacting a compound of Formula (55)

with a compound of Formula (56)

in a solvent containing an additional base and a transition metal catalyst to provide the compound of Formula (54);

wherein:

R 14 is selected from —OH and —OR 17 ;

R 16 is selected from —OH, —H, and —OR 17 ;

the 6,7 bond, the 7,8 bond, and the 8,14 bond are each independently a single bond or a double bond, with the provisos that (1) if the 6,7 bond is a double bond, then the 7,8 bond is a single bond, (2) if the 7,8 bond is a double bond, then the 6,7 and 8,14 bonds are each a single bond, and (3) if the 8,14 bond is a double bond, then the 7,8 bond is a single bond and R 16 is not present;

R 15 is selected from —OH, —H, —OR 17 , ═O, and ═CH 2 with the proviso that if the 6,7 bond is a double bond, then R 15 is selected from —OH, —H, and —OR 17 ;

R 22 is —OC(O)X;

X is selected from —Cl, —Br, and —I; and

R 17 is an oxygen protecting group.

2. The method of claim 1 , wherein the transition metal catalyst comprises a transition metal selected from the group consisting of Pd[0], Pd[II], Ni[0], Ni[II], Ru[II], and combinations of two or more thereof.

3. The method of claim 2 , wherein the transition metal catalyst is selected from the group consisting of Pd(PPh 3 ) 4 , Pd(Ph 2 P(CH 2 ) 4 PPh 2 ) 2 , Ni(PPh 3 ) 4 , Ni(Ph 2 P(CH 2 ) 4 PPh 2 ) 2 , ((pentamethylcyclopentadienyl)RuCl) 4 , [Pd(DBA) 2 ]/PPh 3 , [Pd(OAc) 2 ]/PPh 3 , [Ni(COD) 2 ]/PPh 3 , NiCl 2 /PPh 3 , Ni[P(OEt) 3 ] 4 , and combinations of two or more thereof.

4. The method of claim 1 , wherein the additional base is selected from the group consisting of NaBO 3 , Na 2 HPO 4 , Na 3 PO 4 , K 2 HPO 4 , K 3 PO 4 , NaHCO 3 , KHCO 3 , NaOH, KOH, Na 2 CO 3 , K 2 CO 3 , Cs 2 CO 3 , pyridine, triethylamine, di-iso-propylethylamine, N-methylmorpholine, N,N-dimethylaminopyridine, N-(2-acetamido)-2-aminoethane sulfonic acid, N-(2-acetamido)-iminodiacetic acid, N,N-bis(2-hydroxyethyl)glycine, 3-(cyclohexylamino)-1-propanesulfonic acid, 2-(cyclohexylamino) ethanesulfonic acid, 4-(2-hydroxyethyl)-1-piperazinepropanesulfonic acid, 4-(2-hydroxyethyl)piperazine-1-ethanesulfonic acid, 2-(4-morpholinyl) ethanesulfonic acid, 4-morpholinepropanesulfonic acid, 1,4-piperazinediethanesulfonic acid, [(2-hydroxy-1,1-bis(hydroxymethyl)ethyl)amino]-1-propanesulfonic acid, 2-[(2-hydroxy-1,1-bis(hydroxymethyl)ethyl)amino]ethanesulfonic acid, and combinations of two or more thereof.

5. The method of claim 4 , wherein the additional base is selected from the group consisting of NaHCO 3 , KHCO 3 , Na 2 CO 3 , K 2 CO 3 , Cs 2 CO 3 , triethylamine, di-iso-propylethylamine, and combinations of two or more thereof.

6. The method of claim 1 , wherein:

the R 17 oxygen protecting group is selected from the group consisting of allyl, benzoyl, benzyl, β-methoxyethoxymethyl, dimethoxytrityl, methoxymethyl, para-methoxybenzyl, methylthiomethyl, pivaloyl, tetrahydropyranyl, trityl, trimethylsilyl, tert-butyldimethylsilyl, tert-butyldimethylsilyloxymethyl, tri-iso-propylsilyl, methyl, ethoxyethyl, —C(O)O—CH 2 —CH═CH 2 , tert-butyl-diphenylsilyl, [bis-(4-methoxyphenyl)phenylmethyl)], triphenylmethyl, —C(O)(C 1 -C 4 ) alkyl, —C(O)OR 18 , and —(C 1 -C 6 ) alkyl, each alkyl being unsubstituted or substituted with 1, 2, 3, 4, or 5 independently-selected R 21 groups;

each R 18 independently selected from —(C 1 -C 6 ) alkyl, —(C 2 -C 6 ) alkenyl, and —(C 2 -C 6 ) alkynyl, each alkyl, alkenyl, and alkynyl being unsubstituted or substituted with 1, 2, 3, 4, or 5 independently-selected R 21 groups; and

each R 21 is independently selected from —Cl, —Br, —I, —NH 2 , —CN, and phenyl.

7. The method of claim 6 , wherein the R 17 oxygen protecting group is allyl, benzoyl, benzyl, β-methoxyethoxymethyl, dimethoxytrityl, methoxymethyl, para-methoxybenzyl, methylthiomethyl, pivaloyl, tetrahydropyranyl, trityl, trimethylsilyl, tert-butyldimethylsilyl, tert-butyldimethylsilyloxymethyl, tri-iso-propylsilyl, methyl, ethoxyethyl, or —C(O)O—CH 2 —CH═CH 2 .

8. The method of claim 1 , wherein the 6,7 and 8,14 bonds are each a double bond and R 15 is —OCH 3 .

9. The method of claim 2 , wherein R 14 and R 16 are each —OH, R 15 is ═O, and the 6,7 , 7,8 , and 8,14 bonds are each a single bond.

10. The method of claim 8 , wherein R 14 is —OCH 3 .

11. The method of claim 1 , wherein R 14 and R 16 are each —OH, R 15 is ═O, and the 6,7 , 7,8 , and 8,14 bonds are each a single bond.

12. The method of claim 1 , wherein R 14 is —OCH 3 .

13. The method of claim 1 , wherein the solvent is selected from the group consisting of chloroform, dichloromethane, 1,2-dichloroethane, toluene, tetrahydrofuran, ethyl acetate, acetone, tert-amyl alcohol, tert-butyl alcohol, 3-methyl-3-pentanol, 2,3-dimethyl-3-pentanol, 3-ethyl-pentanol, 2-methyl-2-hexanol, acetonitrile, benzene, carbon tetrachloride, chlorobenzene, 1,2-dichlorobenzene, N,N-dimethylformamide, trifluorotoluene, 1,4-dioxane, 1,2-dimethoxyethane, xylene, and combinations of two or more thereof.

14. The method of claim 13 , wherein the solvent comprises dichloromethane, toluene, tetrahydrofuran, tert-amyl alcohol, acetonitrile, N,N-dimethylformamide, or combinations of two or more thereof.

15. The method of claim 13 , wherein the solvent comprises dichloromethane, toluene, tert-amyl alcohol, N,N-dimethylformamide, or combinations of two or more thereof.

16. The method of claim 2 , wherein the solvent is selected from the group consisting of chloroform, dichloromethane, 1,2-dichloroethane, toluene, tetrahydrofuran, ethyl acetate, acetone, tert-amyl alcohol, tert-butyl alcohol, 3-methyl-3-pentanol, 2,3-dimethyl-3-pentanol, 3-ethyl-pentanol, 2-methyl-2-hexanol, acetonitrile, benzene, carbon tetrachloride, chlorobenzene, 1,2-dichlorobenzene, N,N-dimethylformamide, trifluorotoluene, 1,4-dioxane, 1,2-dimethoxyethane, xylene, and combinations of two or more thereof.

17. The method of claim 16 , wherein the solvent comprises dichloromethane, toluene, tetrahydrofuran, tert-amyl alcohol, acetonitrile, N,N-dimethylformamide, or combinations of two or more thereof.

18. The method of claim 16 , wherein the solvent comprises dichloromethane, toluene, tert-amyl alcohol, N,N-dimethylformamide, or combinations of two or more thereof.

19. The method of claim 4 , wherein the solvent is selected from the group consisting of chloroform, dichloromethane, 1,2-dichloroethane, toluene, tetrahydrofuran, ethyl acetate, acetone, tert-amyl alcohol, tert-butyl alcohol, 3-methyl-3-pentanol, 2,3-dimethyl-3-pentanol, 3-ethyl-pentanol, 2-methyl-2-hexanol, acetonitrile, benzene, carbon tetrachloride, chlorobenzene, 1,2-dichlorobenzene, N,N-dimethylformamide, trifluorotoluene, 1,4-dioxane, 1,2-dimethoxyethane, xylene, and combinations of two or more thereof.

20. The method of claim 19 , wherein the solvent comprises dichloromethane, toluene, tetrahydrofuran, tert-amyl alcohol, acetonitrile, N,N-dimethylformamide, or combinations of two or more thereof.

21. The method of claim 19 , wherein the solvent comprises dichloromethane, toluene, tert-amyl alcohol, N,N-dimethylformamide, or combinations of two or more thereof.

22. The method of claim 6 , wherein the solvent is selected from the group consisting of chloroform, dichloromethane, 1,2-dichloroethane, toluene, tetrahydrofuran, ethyl acetate, acetone, tert-amyl alcohol, tert-butyl alcohol, 3-methyl-3-pentanol, 2,3-dimethyl-3-pentanol, 3-ethyl-pentanol, 2-methyl-2-hexanol, acetonitrile, benzene, carbon tetrachloride, chlorobenzene, 1,2-dichlorobenzene, N,N-dimethylformamide, trifluorotoluene, 1,4-dioxane, 1,2-dimethoxyethane, xylene, and combinations of two or more thereof.

23. The method of claim 22 , wherein the solvent comprises dichloromethane, toluene, tetrahydrofuran, tert-amyl alcohol, acetonitrile, N,N-dimethylformamide, or combinations of two or more thereof.

24. The method of claim 22 , wherein the solvent comprises dichloromethane, toluene, tert-amyl alcohol, N,N-dimethylformamide, or combinations of two or more thereof.

25. The method of claim 8 , wherein the solvent is selected from the group consisting of chloroform, dichloromethane, 1,2-dichloroethane, toluene, tetrahydrofuran, ethyl acetate, acetone, tert-amyl alcohol, tert-butyl alcohol, 3-methyl-3-pentanol, 2,3-dimethyl-3-pentanol, 3-ethyl-pentanol, 2-methyl-2-hexanol, acetonitrile, benzene, carbon tetrachloride, chlorobenzene, 1,2-dichlorobenzene, N,N-dimethylformamide, trifluorotoluene, 1,4-dioxane, 1,2-dimethoxyethane, xylene, and combinations of two or more thereof.

26. The method of claim 25 , wherein the solvent comprises dichloromethane, toluene, tetrahydrofuran, tert-amyl alcohol, acetonitrile, N,N-dimethylformamide, or combinations of two or more thereof.

27. The method of claim 25 , wherein the solvent comprises dichloromethane, toluene, tert-amyl alcohol, N,N-dimethylformamide, or combinations of two or more thereof.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2021
From: RHODES TECHNOLOGIES
To: NORAMCO, LLC
Reel/Frame 055627/0662 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 4, 2015
From: GIGUERE, JOSHUA R.; MCCARTHY, KEITH E.; REISCH, HELGE A.; SANDOVAL, SERGIO; STYMIEST, JAKE L.
To: PURDUE PHARMA L.P.
Reel/Frame 036960/0605 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 4, 2015
From: PURDUE PHARMA L.P.
To: RHODES TECHNOLOGIES
Reel/Frame 036960/0863 →
Continuity (4)
Division 13711520 · Dec 11, 2012
Continuation PCTIB2011001330 · Jun 10, 2011
Provisional Application 61354036 · Jun 11, 2010
Related Publication 20150353567A1 · Dec 10, 2015