CA2194080A1 - Procede de preparation de derives de l'ester de l'oxime de l'acide 2,6-di(4,6-dimethoxypyrimidin-2-yl) oxybenzoique - Google Patents

Procede de preparation de derives de l'ester de l'oxime de l'acide 2,6-di(4,6-dimethoxypyrimidin-2-yl) oxybenzoique

Info

Publication number: CA2194080A1
Authority: CA; Canada
Prior art keywords: alkyl; preparing; see; oxime ester; following formula
Prior art date: 1995-12-28
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Granted

Application number

CA2194080A

Other languages

English (en)

Other versions

CA2194080C (fr

Inventor

Kun-Tai Kim

Byoung-Bae Lee

Goon-Ho Joe

Sei-Chang Ahn

Chang-Mo Kang

Seong-Min Lee

Jae-Soon Bae

Jin-Ho Cho

Sang-Ho Lee

Nak-Hee Choi

Jong-Sin Sa

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

LG Corp

Original Assignee

LG Chemical Co Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1995-12-28

Filing date

1996-12-27

Publication date

1997-06-29

1996-02-05 Priority claimed from KR1019960002737A external-priority patent/KR100209293B1/ko

1996-10-01 Priority claimed from KR1019960043480A external-priority patent/KR100361825B1/ko

1996-12-27 Application filed by LG Chemical Co Ltd filed Critical LG Chemical Co Ltd

1997-06-29 Publication of CA2194080A1 publication Critical patent/CA2194080A1/fr

2000-04-18 Application granted granted Critical

2000-04-18 Publication of CA2194080C publication Critical patent/CA2194080C/fr

2016-12-27 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

-1 2,6-di(4,6-dimethoxypyrimidin-2-yl) oxybenzoic acid oxime ester Chemical class 0.000 title abstract 2
238000004519 manufacturing process Methods 0.000 title abstract 2
125000000217 alkyl group Chemical group 0.000 abstract 4
229910052736 halogen Inorganic materials 0.000 abstract 3
150000002367 halogens Chemical class 0.000 abstract 3
229910052739 hydrogen Inorganic materials 0.000 abstract 3
239000001257 hydrogen Substances 0.000 abstract 3
125000003545 alkoxy group Chemical group 0.000 abstract 2
125000004414 alkyl thio group Chemical group 0.000 abstract 2
125000004093 cyano group Chemical group *C#N 0.000 abstract 2
150000002431 hydrogen Chemical class 0.000 abstract 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
BSLXMJNFHRSKBO-UHFFFAOYSA-N 2,6-bis[(4,6-dimethoxypyrimidin-2-yl)oxy]-N-hydroxybenzamide Chemical compound COC1=NC(=NC(=C1)OC)OC1=C(C(O)=NO)C(=CC=C1)OC1=NC(=CC(=N1)OC)OC BSLXMJNFHRSKBO-UHFFFAOYSA-N 0.000 abstract 1
125000002252 acyl group Chemical group 0.000 abstract 1
125000004423 acyloxy group Chemical group 0.000 abstract 1
229910052783 alkali metal Inorganic materials 0.000 abstract 1
125000003302 alkenyloxy group Chemical group 0.000 abstract 1
125000005092 alkenyloxycarbonyl group Chemical group 0.000 abstract 1
125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 1
125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
125000003118 aryl group Chemical group 0.000 abstract 1
125000005101 aryl methoxy carbonyl group Chemical group 0.000 abstract 1
125000004391 aryl sulfonyl group Chemical group 0.000 abstract 1
125000004104 aryloxy group Chemical group 0.000 abstract 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
150000001875 compounds Chemical class 0.000 abstract 1
125000000753 cycloalkyl group Chemical group 0.000 abstract 1
150000002148 esters Chemical class 0.000 abstract 1
230000002363 herbicidal effect Effects 0.000 abstract 1
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
238000000034 method Methods 0.000 abstract 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
150000003230 pyrimidines Chemical class 0.000 abstract 1

Landscapes

Plural Heterocyclic Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

CA 2194080 1995-12-28 1996-12-27 Procede de preparation de derives de l'ester de l'oxime de l'acide 2,6-di(4,6-dimethoxypyrimidin-2-yl) oxybenzoique Expired - Fee Related CA2194080C (fr)

Applications Claiming Priority (6)

Application Number	Priority Date	Filing Date	Title
KR19950061160		1995-12-28
KR95-61160		1995-12-28
KR1019960002737A KR100209293B1 (ko)	1996-02-05	1996-02-05	제초성 피리미딜옥시벤조산 옥심에스테르 유도체의 신규한 제조방법
KR96-2737		1996-02-05
KR96-43480		1996-10-01
KR1019960043480A KR100361825B1 (ko)	1996-10-01	1996-10-01	치환된 5-(4,6-디메톡시피리미딘-2-일)옥시-4h-(1,3)-벤조디옥신-4-온 유도체를 이용한 제초성 피리미딜옥시 벤조산 옥심에스테 르 유도체의 제조방법

Publications (2)

Publication Number	Publication Date
CA2194080A1 true CA2194080A1 (fr)	1997-06-29
CA2194080C CA2194080C (fr)	2000-04-18

Family

ID=27349271

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA 2194080 Expired - Fee Related CA2194080C (fr)	1995-12-28	1996-12-27	Procede de preparation de derives de l'ester de l'oxime de l'acide 2,6-di(4,6-dimethoxypyrimidin-2-yl) oxybenzoique

Country Status (4)

Country	Link
AR (1)	AR005300A1 (fr)
CA (1)	CA2194080C (fr)
CO (2)	CO4560535A1 (fr)
MX (1)	MX9606690A (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2000061573A1 (fr) *	1999-04-14	2000-10-19	Rhodia Chimie	Nouvelles benzodioxinones et leur procede d'obtention
CN103319421A (zh) *	2013-06-07	2013-09-25	常州大学	一种嘧啶水杨酸类除草剂嘧啶肟草醚的制备方法
CN103333121A (zh) *	2013-07-22	2013-10-02	金坛市信德农业科技有限公司	具有除草活性的氟嘧肟草醚类化合物及其制备方法
CN104302629A (zh) *	2013-12-03	2015-01-21	南京慧博生物科技有限公司	新型除草活性的嘧啶水杨酸类化合物、其制备方法及其作为除草剂的用途
CN108383827A (zh) *	2018-03-29	2018-08-10	中山大学	一种苯并1,3-二噁英-4酮类缩醛化合物的制备方法

1996
- 1996-12-19 MX MX9606690A patent/MX9606690A/es unknown
- 1996-12-27 CA CA 2194080 patent/CA2194080C/fr not_active Expired - Fee Related
- 1996-12-27 AR ARP960105922A patent/AR005300A1/es active IP Right Grant
- 1996-12-27 CO CO96068262D patent/CO4560535A1/es unknown
- 1996-12-27 CO CO96068262A patent/CO4560533A1/es unknown

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2000061573A1 (fr) *	1999-04-14	2000-10-19	Rhodia Chimie	Nouvelles benzodioxinones et leur procede d'obtention
FR2792315A1 (fr) *	1999-04-14	2000-10-20	Rhodia Chimie Sa	Nouvelles benzodioxinones et leur procede d'obtention
CN103319421A (zh) *	2013-06-07	2013-09-25	常州大学	一种嘧啶水杨酸类除草剂嘧啶肟草醚的制备方法
CN103319421B (zh) *	2013-06-07	2016-06-08	常州大学	一种嘧啶水杨酸类除草剂嘧啶肟草醚的制备方法
CN103333121A (zh) *	2013-07-22	2013-10-02	金坛市信德农业科技有限公司	具有除草活性的氟嘧肟草醚类化合物及其制备方法
CN105272924A (zh) *	2013-07-22	2016-01-27	金坛市信德农业科技有限公司	具有除草活性的氟嘧啶草醚类化合物及其制备方法
CN105272924B (zh) *	2013-07-22	2016-08-17	金坛市信德农业科技有限公司	具有除草活性的氟嘧啶草醚类化合物及其制备方法
CN104302629A (zh) *	2013-12-03	2015-01-21	南京慧博生物科技有限公司	新型除草活性的嘧啶水杨酸类化合物、其制备方法及其作为除草剂的用途
WO2015081493A1 (fr) *	2013-12-03	2015-06-11	南京慧博生物科技有限公司	Composé de salicylate de pyrimidyle présentant une nouvelle activité herbicide, procédé de préparation correspondant et utilisations correspondantes comme herbicide
CN108383827A (zh) *	2018-03-29	2018-08-10	中山大学	一种苯并1,3-二噁英-4酮类缩醛化合物的制备方法

Also Published As

Publication number	Publication date
CO4560535A1 (es)	1998-02-10
AR005300A1 (es)	1999-04-28
CA2194080C (fr)	2000-04-18
CO4560533A1 (es)	1998-02-10
MX9606690A (es)	1997-06-28

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Legal Events

Date	Code	Title	Description
1996-12-27	EEER	Examination request
2015-02-09	MKLA	Lapsed	Effective date: 20141229