IP Library Granted Patent US 11,136,292
Granted Patent B2
US 11,136,292 · App. 16/332,673 · Granted Oct 5, 2021

Plant growth regulator compounds

Inventors: Alexandre Franco Jean Camille Lumbroso (Stein, CH); Alain De Mesmaeker (Stein, CH); Claudio Screpanti (Stein, CH); Stefano Rendine (Stein, CH)
Assignee: SYNGENTA PARTICIPATIONS AG
C07D207/38A01N43/08A01N43/12A01N43/16A01N43/30A01N43/36A01N43/54A01N43/76C07D307/58C07D307/60C07D403/12C07D407/12C07D409/12C07D413/12
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Quick Facts
Patent No.
US 11,136,292
App. No.
16/332,673
Granted
Oct 5, 2021
Kind
B2
Abstract

The present invention relates to relates to novel strigolactone derivatives of formula (I), to processes for preparing these derivatives including intermediate compounds, to seeds comprising these derivatives, to plant growth regulator or seed germination promoting compositions comprising these derivatives and to methods of using these derivatives in controlling the growth of plants and/or promoting the germination of seeds.

Claims (22)

1. A compound of formula (I)

wherein

R 1 and R 2 are independently selected from the group consisting of hydrogen, C 1 -C 3 alkyl and C 1 -C 3 alkoxy;

X is O(R 3 );

R 3 is selected from the group consisting of hydrogen and C 1 -C 4 alkyl;

Y is O;

Z is selected from the group consisting of a bond, CH 2 , CH 2 -CH 2 , CH 2 (wherein the oxygen atom is bonded to the carbon positioned alpha to the A 1 substituent) and oxygen;

A 1 to A 4 are each independently selected from the group consisting of a bond, CR 8 , N, S and O, wherein A 1 to A 4 together with the atoms to which they are joined form a 5 to 6 membered aryl or heteroaryl; and

each R 8 is selected from the uroup consisting of hydrogen, halogen, methyl, ethyl, methoxy, ethoxy, fluoromethyl and trifluoromethyl; or two R 8 groups are joined via —OCH 2 O—to form a dioxolane ring;

or salts thereof.

2. A compound according to claim 1 , wherein R 1 and R 2 are independently selected from the group consisting of hydrogen, methyl, ethyl and methoxy.

3. A compound according to claim 1 , wherein R 1 is methyl and R 2 is hydrogen or methyl.

4. A compound according to claim 3 , wherein R 2 is methyl.

5. A compound according to claim 1 , wherein R 3 is selected from the group consisting of hydrogen, methyl and ethyl.

6. A compound according to claim 1 , wherein A 1 to A 4 are each independently selected from the group consisting of a bond, CR 8 , N, S and O, and A 1 to A 4 together with the atoms to which they are joined form a 5 to 6 membered aryl or heteroaryl.

7. A compound according to claim 1 , wherein A 1 to A 4 are each CR 8 .

8. A composition comprising a compound according to claim 1 , and an agriculturally acceptable formulation adjuvant.

9. A mixture comprising a compound as defined in claim 1 , and a further active ingredient.

10. A crop yield enhancing composition, comprising a compound according to claim 1 .

11. A method for improving the tolerance of a plant to abiotic stress, promoting seed germination of a plant, or regulating or improving the growth of a plant, wherein the method comprises applying to the plant, plant part, plant propagation material, or plant growing locus a compound according to claim 1 .

12. A compound according to claim 1 , wherein Z is CH 2 .

13. A compound according to claim 1 , selected from: ethyl (E)-2-indan-1 -yl-3-[(4-methyl-5-oxo-2H-furan-2-yl)oxy]prop-2-enoate; ethyl (E)-3-[(3,4-dimethyl-5-oxo-2H-furan-2-yl)oxy]-2-indan-l-yl-prop-2-enoate; methyl (E)-2-indan-l-yl-3-[(4-methyl-5-oxo-2H-furan-2-yl)oxy]prop-2-enoate; methyl (E)-3-[(3,4-dimethyl-5-oxo-2H-furan-2-yl)oxy]-2-indan-l-yl-prop-2-enoate; ethyl (E)-2-(5,6-dimethoxyindan-l-yl)-3-[(4-methyl-5-oxo-2H-furan-2-yl)oxy]prop-2-enoate; ethyl (E)-2-(5,6-dimethoxyindan-1 -yl)-3-[(3,4-dimethyl-5-oxo-2H-furan-2-yl)oxy]prop-2-enoate; ethyl (E)-2-(6,7-dihydro-5H-cyclopenta[f[[1,3]benzodioxol-7-yl)-3-[(4-methyl-5-oxo-2H-furan-2-y 1)oxy]prop-2-enoate; ethyl (E)-2-(4-methylindan-l-yl)-3-[(4-methyl-5-oxo-2H-furan-2-yl)oxy]prop-2-enoate; ethyl (E)-3-[(4-methyl-5-oxo-2H-furan-2-yl)oxy]-2-[4-(trifluoromethyl)indan-l-yl]prop-2-enoate; ethyl (E)-3-[(3,4-dimethyl-5-oxo-2H-furan-2-yl)oxy]-2-(6-hydroxyindan-l-yl)prop-2-enoate; ethyl (E)-3-[(3,4-dimethyl-5-oxo-2H-furan-2-yl)oxy]-2-tetralin-l-yl-prop-2-enoate; ethyl (E)-2-(7-bicyclo[4.2.0]octa-l(6),2,4-trienyl)-3-[(4-methyl-5-oxo-2H-furan-2-yl)oxy]prop-2-enoate; ethyl (E)-2-(5,6-dihydro-4H-cyclopenta[b]thiophen-6-yl)-3-[(3,4-dimethyl-5-oxo-2H-furan-2-yl)oxy]prop-2-enoate; ethyl (E)-2-chroman-4-yl-3-[(4-methyl-5-oxo-2H-furan-2-yl)oxy]prop-2-enoate; ethyl (E)-2-chroman-4-yl-3-[(3,4-dimethyl-5-oxo-2H-furan-2-yl)oxy]prop-2-enoate; and ethyl (E)-2-(2,3-dihydrobenzofuran-3-yl)-3-[(3,4-dimethyl-5-oxo-2H-furan-2-yl)oxy]prop-2-enoate.

Assignments (2)
MERGER AND CHANGE OF NAME Recorded Feb 28, 2025
From: SYNGENTA PARTICIPATIONS AG; SYNGENTA PARTICIPATIONS AG
To: SYNGENTA CROP PROTECTION AG
Reel/Frame 070362/0699 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 10, 2019
From: LUMBROSO, ALEXANDRE FRANCO JEAN CAMILLE; DE MESMAEKER, ALAIN; SCREPANTI, CLAUDIO; RENDINE, STEFANO
To: SYNGENTA PARTICIPATIONS AG
Reel/Frame 048848/0818 →