IP Library Granted Patent US 8,198,461
Granted Patent B2
US 8,198,461 · App. 12/437,711 · Granted Jun 12, 2012

Process for the preparation of 3-cyano-1,2,4-triazoles

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Quick Facts
Patent No.
US 8,198,461
App. No.
12/437,711
Granted
Jun 12, 2012
Kind
B2
Abstract

The present invention provides compounds and methods that can be used to convert 1,2,4-triazole-3-carboxamides to the corresponding 3-cyano-1,2,4-triazoles reliably in one step, with high yields and without the need for elaborate purification.

Claims (43)

1. A method for preparing a compound of Formula (I):

or a tautomer or salt thereof; said method comprising dehydrating a compound of Formula (II):

with at least one dehydrating agent selected from the group consisting of trifluoroacetic anhydride, thionyl chloride, and phosphorus oxychloride in at least one solvent selected from the group consisting of acetonitrile, 1,4-dioxane, ethyl acetate, 1-methyl-2-pyrrolidinone, and pyridine; to form a compound of formula (I);

wherein:

X is O or S; and

R 2 is-selected from the group consisting of C 1-8 alkyl, aryl and halogen.

2. The method of claim 1 , wherein X is S.

3. The method of claim 1 , wherein X is O.

4. The method of claim 1 , wherein said dehydrating agent is present in an amount ranging from 2.5 equivalents to 9 equivalents to the amount of the compound of Formula (II).

5. The method of claim 1 , wherein said dehydrating agent is present at a concentration ranging from 3 molar equivalents to 28 molar equivalents to the amount of the compound of Formula (II).

6. The method of claim 1 , wherein said method further comprises carrying out the dehydration at a temperature ranging from 0° C. to 160° C.

7. The method of claim 1 , wherein said method further comprises quenching the reaction with a quenching agent selected from the group consisting of water, NaHCO 3 , Na 2 CO 3 , NaOH, KOH, NH 4 OH, and triethylamine.

8. The method of claim 1 , wherein said dehydrating agent is POCl 3 .

9. The method of claim 1 , wherein the solvent is acetonitrile.

10. The method of claim 1 , wherein the compound of Formula (I) has the structure:

wherein R 2 is selected from the group consisting of H, C 1-8 alkyl, aryl and halogen; or a tautomer or salt thereof; said method comprising dehydrating a compound of Formula (IIai):

by contacting the compound of Formula (IIai) with phosphorus oxychloride in acetonitrile.

11. The method of claim 1 , further comprising producing a salt of the compound of Formula (I).

12. The method of claim 1 , further comprising isolating the compound of Formula (I).

13. The method of claim 1 , wherein said method further comprises an organic base soluble in said reaction mixture.

14. The method of claim 13 , wherein said organic base is pyridine.

15. The method of claim 1 , wherein said method further comprises purifying said compound of Formula (I) by extraction or filtration.

16. The method of claim 15 , wherein said extraction comprises contacting the compound of Formula (I) with a solvent mixture selected from the group consisting of water/ethyl acetate, water/isopropyl acetate and water/2-methyltetrahydrofuran.

17. The method of claim 15 , wherein said filtration comprises contacting the compound of Formula (I) with a solvent in which the compound of Formula (I) is insoluble and filtering the mixture to provide purified compound of Formula (I).

18. The method of claim 17 , wherein the solvent in which the compound of Formula (I) is insoluble is toluene.

19. A method for preparing a compound of Formula (I):

or a tautomer or salt thereof; said method comprising dehydrating a compound of Formula (II):

with at least one dehydrating agent selected from the group consisting of trifluoroacetic anhydride, and thionyl chloride, in at least one solvent selected from the group consisting of acetonitrile, 1,4-dioxane, ethyl acetate, 1-methyl-2-pyrrolidinone, and pyridine; to form a compound of formula (I);

wherein:

X is O or S; and

R 2 is selected from the group consisting of H, C 1-8 alkyl, aryl and halogen.

20. A method for preparing a compound of Formula (I):

or a tautomer or salt thereof; said method comprising dehydrating a compound of Formula (II):

with at least one dehydrating agent selected from the group consisting of trifluoroacetic anhydride, thionyl chloride, and phosphorus oxychloride in at least one solvent selected from the group consisting of 1,4-dioxane, ethyl acetate, 1-methyl-2-pyrrolidinone, and pyridine; to form a compound of formula (I);

wherein:

X is O or S; and

R 2 is selected from the group consisting of C 1-8 alkyl, aryl and halogen.

21. A method for preparing a compound of Formula (I):

or a tautomer or salt thereof; said method comprising dehydrating a compound of Formula (II):

with at least one dehydrating agent selected from the group consisting of trifluoroacetic anhydride, thionyl chloride, and phosphorus oxychloride in at least one solvent selected from the group consisting of acetonitrile, 1,4-dioxane, ethyl acetate, 1-methyl-2-pyrrolidinone, and pyridine; to form a compound of formula (I);

wherein:

X is S; and

R 2 is-selected from the group consisting of H, C 1-8 alkyl, aryl and halogen.

Assignments (10)
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT STATEMENT THAT THIS DOCUMENT SERVES AS AN OATH/DECLARATION PREVIOUSLY RECORDED AT REEL: 047383 FRAME: 0438. ASSIGNOR(S) HEREBY CONFIRMS THE TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS. Recorded Nov 5, 2018
From: KEYBANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: AMPAC FINE CHEMICALS LLC
Reel/Frame 047422/0852 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS Recorded Aug 31, 2018
From: KEYBANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: AMPAC FINE CHEMICALS LLC
Reel/Frame 047383/0437 →
GRANT OF SECURITY INTEREST IN PATENTS Recorded Aug 3, 2018
From: AMPAC FINE CHEMICALS LLC
To: KEYBANK NATIONAL ASSOCIATION
Reel/Frame 046703/0605 →
RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT R/F: 032365/0398 Recorded Dec 15, 2015
From: JEFFERIES FINANCE LLC, AS ADMINISTRATIVE AGENT
To: AMPAC FINE CHEMICALS LLC
Reel/Frame 037300/0399 →
SECURITY AGREEMENT Recorded Feb 27, 2014
From: AMPAC FINE CHEMICALS LLC
To: JEFFERIES FINANCE LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 032365/0398 →
PATENT RELEASE AND REASSIGNMENT (R/F 029370/0835) Recorded Feb 27, 2014
From: KEYBANK NATIONAL ASSOCIATION, AS AGENT
To: AMPAC FINE CHEMICALS LLC
Reel/Frame 032363/0222 →
COLLATERAL ASSIGNMENT AND SECURITY INTEREST OF PATENTS Recorded Nov 28, 2012
From: AMPAC FINE CHEMICALS LLC
To: KEYBANK NATIONAL ASSOCIATION
Reel/Frame 029370/0835 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE FROM AMERICAN FINE CHEMICALS LLC TO AMPAC FINE CHEMICALS LLC PREVIOUSLY RECORDED ON REEL 029203 FRAME 0091. ASSIGNOR(S) HEREBY CONFIRMS THE RELEASE BY SECURED PARTY. Recorded Nov 5, 2012
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: AMPAC FINE CHEMICALS LLC
Reel/Frame 029245/0597 →
RELEASE OF SECURITY INTEREST Recorded Oct 26, 2012
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: AMERICAN FINE CHEMICALS LLC
Reel/Frame 029203/0091 →
SECURITY AGREEMENT Recorded Feb 2, 2011
From: AMPAC FINE CHEMICALS LLC
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS AGENT
Reel/Frame 025732/0985 →