RU2000124062A - Derivatives of 2-pyridylmethylamine, suitable as fungicides - Google Patents
Derivatives of 2-pyridylmethylamine, suitable as fungicidesInfo
- Publication number
- RU2000124062A RU2000124062A RU2000124062/04A RU2000124062A RU2000124062A RU 2000124062 A RU2000124062 A RU 2000124062A RU 2000124062/04 A RU2000124062/04 A RU 2000124062/04A RU 2000124062 A RU2000124062 A RU 2000124062A RU 2000124062 A RU2000124062 A RU 2000124062A
- Authority
- RU
- Russia
- Prior art keywords
- formula
- compounds
- optionally substituted
- hydrogen
- pyridyl
- Prior art date
Links
- 230000000855 fungicidal Effects 0.000 title claims 2
- 239000000417 fungicide Substances 0.000 title claims 2
- WOXFMYVTSLAQMO-UHFFFAOYSA-N 2-Pyridinemethanamine Chemical class NCC1=CC=CC=N1 WOXFMYVTSLAQMO-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 10
- 239000000543 intermediate Substances 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 239000011780 sodium chloride Substances 0.000 claims 3
- 125000000547 substituted alkyl group Chemical group 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 230000003032 phytopathogenic Effects 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 241000233866 Fungi Species 0.000 claims 1
- 206010061217 Infestation Diseases 0.000 claims 1
- 125000002252 acyl group Chemical group 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 230000003993 interaction Effects 0.000 claims 1
- 230000000361 pesticidal Effects 0.000 claims 1
Claims (6)
где А1 является замещенным 2-пиридилом;
А2 является необязательно замещенным фенилом;
L является -(С= O)-; -SO2- или -(C= S)-;
R1 является водородом, необязательно замещенным алкилом или ацилом и
R2 является водородом или необязательно замещенным алкилом и его соли.1. Phytopathogenic fungicide containing compounds of formula I
where a 1 is a substituted 2-pyridyl;
A 2 is optionally substituted phenyl;
L is - (C = O) -; -SO 2 - or - (C = S) -;
R 1 is hydrogen, optionally substituted alkyl or acyl and
R 2 is hydrogen or optionally substituted alkyl and its salts.
и его соли, в которой А1 является 2-пиридилом, имеющим заместители в 3 и/или 5 положении, а не в другом положении. А2 является необязательно замещенным фенилом; R1 и R2 являются водородом, и L является -(С= O)-, -SO2-, -(C= S)-.2. The compound of formula I
and its salt, in which And 1 is 2-pyridyl, having substituents in the 3 and / or 5 position, and not in another position. A 2 is optionally substituted phenyl; R 1 and R 2 are hydrogen, and L is - (C = O) -, -SO 2 -, - (C = S) -.
включающий стадии:
а) взаимодействия в щелочных условиях соединений формулы IV с соединениями формулы V для получения промежуточных соединений формулы VI
b) превращения промежуточных соединений формулы VI в промежуточные соединения формулы VII
с) превращения промежуточных соединений формулы VII в соединения формулы IIа
где Ra и Rb, которые могут быть одинаковыми или различными, являются алкилом, алкенилом, алкинилом, циклоалкилом, циклоалкенилом, гетероциклилом или фенилом, каждый из которых может быть замещенным;
Е1 является как группой - акцептором электронов, так и группой, которая может замещаться водородом известным путем согласно стадии с);
X1 является уходящей группой и
А1 и R1 определены в п. 1.5. The method of obtaining the intermediate compounds of formula IIa
including stages:
a) interaction under alkaline conditions of compounds of formula IV with compounds of formula V to obtain intermediate compounds of formula VI
b) converting intermediates of formula VI to intermediates of formula VII
c) converting intermediates of formula VII to compounds of formula IIa
where R a and R b , which may be the same or different, are alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, heterocyclyl or phenyl, each of which may be substituted;
E 1 is both an electron acceptor group and a group that can be replaced by hydrogen in a known manner according to step c);
X 1 is a leaving group and
A 1 and R 1 are defined in paragraph 1.
его соли, где А1 является 2-пиридил, имеющий заместители в 3 и/или 5 положении, и R1 является необязательно замещенным алкилом, в качестве промежуточного продукта.6. The compound of formula IIb and
its salts, where A 1 is 2-pyridyl, having substituents in the 3 and / or 5 position, and R 1 is an optionally substituted alkyl, as an intermediate product.
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB9803413.5A GB9803413D0 (en) | 1998-02-19 | 1998-02-19 | Fungicides |
GB9803413.5 | 1998-02-19 | ||
GBGB9813998.3A GB9813998D0 (en) | 1998-06-30 | 1998-06-30 | Fungicides |
GB9813998.3 | 1998-06-30 | ||
GB9817353.7 | 1998-08-11 | ||
GBGB9817353.7A GB9817353D0 (en) | 1998-08-11 | 1998-08-11 | Fungicides |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2000124062A true RU2000124062A (en) | 2002-08-27 |
RU2224746C2 RU2224746C2 (en) | 2004-02-27 |
Family
ID=27269216
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2000124062/04A RU2224746C2 (en) | 1998-02-19 | 1999-02-16 | Phytopathogenic fungicide, derivative of 2-pyridylmethylamine, fungicide composition, method for control of phytopathogenic fungi |
Country Status (29)
Country | Link |
---|---|
US (2) | US6503933B1 (en) |
EP (1) | EP1056723B1 (en) |
JP (1) | JP4749542B2 (en) |
KR (1) | KR100603172B1 (en) |
CN (1) | CN1132816C (en) |
AR (1) | AR017459A1 (en) |
AU (1) | AU751032B2 (en) |
BR (2) | BR9908007B1 (en) |
CA (1) | CA2319005C (en) |
CZ (1) | CZ298746B6 (en) |
DE (1) | DE69937633T2 (en) |
DK (1) | DK1056723T3 (en) |
ES (1) | ES2293717T3 (en) |
HU (1) | HU229030B1 (en) |
ID (1) | ID26626A (en) |
IL (3) | IL137573A0 (en) |
NO (1) | NO317105B1 (en) |
NZ (1) | NZ505954A (en) |
PL (1) | PL194057B1 (en) |
PT (1) | PT1056723E (en) |
RO (1) | RO120970B1 (en) |
RS (1) | RS50017B (en) |
RU (1) | RU2224746C2 (en) |
SI (1) | SI20356B (en) |
SK (1) | SK286310B6 (en) |
TR (2) | TR200101071T2 (en) |
TW (1) | TW575562B (en) |
UA (1) | UA72204C2 (en) |
WO (1) | WO1999042447A1 (en) |
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