IP Library Granted Patent US 8,487,112
Granted Patent B2
US 8,487,112 · App. 12/677,778 · Granted Jul 16, 2013

Method for producing 4-aminobut-2-enolides

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Quick Facts
Patent No.
US 8,487,112
App. No.
12/677,778
Granted
Jul 16, 2013
Kind
B2
Abstract

The present invention relates to a process for preparing 4-aminobut-2-enolides and also corresponding intermediates and starting compounds which are passed through or used in the process according to the invention.

Claims (37)

1. A process for preparing an 4-aminobut-2-enolide of formula (I)

in which

A is pyrid-2-yl or pyrid-4-yl or is pyrid-3-yl which is optionally 6-substituted by fluorine, chlorine, bromine, methyl, trifluoromethyl or trifluoromethoxy, or is a

 radical

in which

X is halogen, alkyl or haloalkyl, and

Y is halogen, alkyl, haloalkyl, haloalkoxy, azido or cyano, and

R 1 is alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, halocycloalkyl, alkoxy, alkoxyalkyl, halocycloalkylalkyl or arylalkyl,

comprising reacting a 4-haloacetoacetic ester of formula (II)

in which

R 2 is C 1 -C 12 -alkyl, C 5 -C 8 -aryl or arylalkyl, and

Hal is Cl, Br or I,

in the presence of a solvent at a temperature of from −20° C. to 60° C.,

a) with an amine of formula (IIIa)

in which R 1 is as defined above,

to give a compound of formula (IVa)

followed by

removing the solvent by distillation or under reduced pressure in a temperature range of from 20° C. to 35° C.,

thermally cyclizing the compound of formula (IVa) in the presence of a solvent at a temperature of from 40° C. to 150° C. to give a compound of formula (Va)

isolating the compound of formula (Va) by crystallization or removal of solvent, and reacting the compound of formula (Va) with a compound of the formula (VIa)

A-CH 2 -E  (VIa)

where A is as defined above and E is a leaving group selected from the group consisting of chlorine, bromine, iodine, mesylate, tosylate, or SO 2 CH 3 ,

to give compound (I);

or

b) with an amine of formula (IIIb)

H 2 N-CH 2 -A  (IIIb)

in which A is as defined above,

to give a compound of formula (IVb)

followed by

removing the solvent by distillation or under reduced pressure in a temperature range of from 20° C. to 35° C.,

thermally cyclizing the compound of formula (IVb) in the presence of a solvent at a temperature of from 40° C. to 150° C. to give a compound of formula (Vb)

isolating the compound of formula (Vb) by crystallization or removal of solvent, and reacting the compound of formula (Vb) with a compound of formula (VIb)

R 1 -E  (VIb)

where R 1 is as defined above and E is a leaving group selected from the group consisting of chlorine, bromine, iodine, mesylate, tosylate, or SO 2 CH 3 ,

to give compound (I).

2. A process according to claim 1 wherein the reaction of the compound of formula (Va) with the compound of formula (VIa) or the reaction of the compound of formula (Vb) with the compound of formula (VIb) is carried out in the presence of a base.

3. A process according to claim 2 wherein the base is sodium hydroxide or potassium hydroxide.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE ADDRESS PREVIOUSLY RECORDED AT REEL: 034891 FRAME: 0140. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Feb 19, 2015
From: BAYER CROPSCIENCE AG
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 035046/0921 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 3, 2015
From: BAYER CROPSCIENCE AG
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 034891/0140 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 11, 2010
From: LUI, NORBERT; HEINRICH, JENS-DIETMAR
To: BAYER CROPSCIENCE AG
Reel/Frame 024069/0446 →