JPH0123472B2 - - Google Patents

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Publication number
JPH0123472B2
JPH0123472B2 JP4796783A JP4796783A JPH0123472B2 JP H0123472 B2 JPH0123472 B2 JP H0123472B2 JP 4796783 A JP4796783 A JP 4796783A JP 4796783 A JP4796783 A JP 4796783A JP H0123472 B2 JPH0123472 B2 JP H0123472B2
Authority
JP
Japan
Prior art keywords
parts
compound
formula
halogen atom
present
Prior art date
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.)
Expired
Application number
JP4796783A
Other languages
Japanese (ja)
Other versions
JPS59175489A (en
Inventor
Hiroshi Sugyama
Keizo Hosoda
Yoshikazu Kumagai
Masaki Takeuchi
Masanori Okada
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.)
Chugai Pharmaceutical Co Ltd
Original Assignee
Chugai Pharmaceutical 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.)
Filing date
Publication date
Application filed by Chugai Pharmaceutical Co Ltd filed Critical Chugai Pharmaceutical Co Ltd
Priority to JP4796783A priority Critical patent/JPS59175489A/en
Priority to US06/589,018 priority patent/US4596801A/en
Priority to CA000449586A priority patent/CA1228590A/en
Priority to AU25806/84A priority patent/AU562226B2/en
Priority to DE8484103191T priority patent/DE3464608D1/en
Priority to AT84103191T priority patent/ATE28198T1/en
Priority to EP84103191A priority patent/EP0120480B1/en
Priority to ES530959A priority patent/ES8604947A1/en
Priority to BR8401360A priority patent/BR8401360A/en
Publication of JPS59175489A publication Critical patent/JPS59175489A/en
Priority to ES544241A priority patent/ES8604194A1/en
Publication of JPH0123472B2 publication Critical patent/JPH0123472B2/ja
Granted legal-status Critical Current

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  • Plural Heterocyclic Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、一般式〔〕 (但し式中、Xは水素原子又はハロゲン原子を
示し、Yはハロゲン原子を示し、mは0〜2の整
数を示す。) で表わされる4H−3,1−ベンゾオキサジン誘
導体、その製造法およびそれら4H−3,1−ベ
ンゾオキサジン誘導体の1種又は2種以上を含有
することを特徴とする農園芸用殺菌剤に関するも
のである。 すでに殺菌性を有する合成有機化合物、抗生物
質が数多く見出され農園芸用殺菌剤として開発さ
れた物質も多い。 しかし、近年耐性菌の出現や大量散布による環
境汚染が問題となりつつある。 又、近年、農園芸用殺菌剤として所謂アゾール
系化合物に関する発明が数多く発表されている。
例えば特開昭56−152446、特開昭57−16870、特
開昭57−48982、特開昭57−120579、特開昭57−
126479がある。 しかし、これらの化合物は植物生長抑制作用や
除草作用を有することが多く、必らずしも安全に
使用出来る薬剤とは言えない欠点がある。 本発明者らは、これらの欠点を補うことを目的
として、新規な骨格を有し、しかも少量でも強い
効果を示す薬剤の開発に鋭意努力し本発明を完成
した。 一般式〔〕で表わされる本発明化合物は、新
規な化合物であり、有用な栽培作物の病害に対し
てすぐれた作用を示し、人畜、魚類に対しては高
い安全性をもち、作物に対しては何の悪影響も示
さないものである。 一般式〔〕で表わされる本発明化合物は、農
園芸用殺菌剤として、そう菌類、子のう菌類、担
子菌類および不完全菌類等に属する各種病原菌に
対して予防、治療の両面で広範囲に適用すること
が出来る。特に有用植物のうどんこ病、さび病等
には優れた効力を示すものである。 一般式〔〕で表わされる本発明化合物は一般
式〔〕 (但し式中、Xは水素原子又はハロゲン原子を
示し、Yはハロゲン原子を示し、mは0〜2の整
数を示す。) で表わされるアミノベンズヒドロール誘導体を閉
環することにより製造することが出来る。 なお、一般式〔〕で表わされるアミノベンズ
ヒドロール誘導体は例えば特開昭57−59867等で
公知である。 一般式〔〕で表わされるアミノベンズヒドロ
ール誘導体は、所謂ハロゲン化剤、例えば塩化チ
オニル、臭化チオニル、三塩化リン、三臭化リ
ン、五塩化リン等を使用することにより閉環さ
せ、4H−3,1−ベンゾオキサジン誘導体〔〕
を製造することが出来る。この閉環反応を収率よ
く行うためにはピリジン、トリエチルアミン、ジ
アルキルアミン等の脱酸剤を使用することがより
好ましい。 又、反応を円滑に進行させるためには適当な溶
媒を使用してもよい。先に示した脱酸剤は何れも
液体であり、脱酸剤としての作用の他に過剰に使
用することにより溶媒としての作用も同時にもた
せることが出来ることは当然であるが、溶媒のみ
の作用をもたせるものとして例えばベンゼン、ト
ルエン、クロロホルム等を用いることが出来る。 反応温度はなんら特別の操作も要しない室温で
充分であるが、一般的には−5℃〜30℃であり好
ましくは0℃〜20℃である。 次に製造例を示して説明する。 なお、本発明化合物〔〕の骨核の位置表示
(ナンバーリング)は下記の通りである。 製造例 1 4−(4′−クロロフエニル)−2−(4−ピリジ
ル)−4H−3,1−ベンゾオキサジン(化合物
番号4) ピリジン200mlに氷冷下、2−(4−クロロ−α
−ヒドロキシベンジル)−イソニコチンアニリド
11.3gを加え、更に塩化チオニル4gを徐々に加
え1時間撹拌した。室温下更に撹拌反応させたの
ち反応混合物を水中に注ぐと結晶が析出した。得
られた結晶を別後酢酸エチルエステルに溶か
し、水洗したのち、酢酸エチルエステル溶液を無
水芒晶で乾燥した。無水芒晶を別し減圧下酢酸
エチルエステルを溜去し、酢酸エチルエステル−
n−ヘキサン混合溶媒で再結晶すると、目的物の
結晶9.8g(収率92%)を得た。融点116〜117℃。 元素分析値:C19H13ClN2O分子量320.77として C H N 計算値(%) 71.14 4.08 8.73 実測値(%) 71.19 4.01 8.70 製造例 2 4−(4′−クロロフエニル)−6−フルオロ−2
−(4−ピリジル)−4H−3,1−ベンゾオキ
サジン(化合物番号11) 2−(4−クロロ−α−ヒドロキシベンジル)−
4−フルオロ−イソニコチンアニリド11.9gを用
い製造例1と同様に操作し目的物10.2g(収率90
%)を得た。融点144〜145℃。 元素分析値:C19H12ClFN2O分子量338.77とし
て C H N 計算値(%) 67.36 3.57 8.27 実測値(%) 67.31 3.62 8.23 製造例 3 6−クロロ−4−(4′−クロロフエニル)−2−
(4−ピリジル)−4H−3,1−ベンゾオキサ
ジン(化合物番号8) クロロホルム300ml中に4−クロロ−2−(4−
クロロ−α−ヒドロキシベンジル)−イソニコチ
ンアニリド12.4gとトリエチルアミン5.0mlを溶
かし、氷冷撹拌下、三臭化リン9.1gを徐々に加
えたのち、1時間撹拌を続けた。室温で3時間更
に撹拌を続けたのち、反応混合物を水中に注ぐ。
クロロホルム層をよく水洗したのち乾燥した。減
圧下クロロホルムを完全に溜去したのち酢酸エチ
ルエステル−n−ヘキサン混合溶媒から再結晶し
て目的物10.1g(収率85%)を得た。融点140〜
141℃。 元素分析値:C19H12Cl2N2O分子量352.23とし
て C H N 計算値(%) 64.24 3.41 7.89 実測値(%) 64.29 3.38 7.91 製造例 4 6−ブロモ−4−フエニル−2−(4−ピリジ
ル)−4H−3,1−ベンゾオキサジン(化合物
番号3) 製造例3の方法に従い、4−ブロモ−2−(α
−ヒドロキシベンジル)−イソニコチンアニリド
12.8gを用い、トリエチルアミンの代りにジエチ
ルアニリン6.0mlを用いて反応させて、目的物
10.3g(収率85%)を得た。融点161〜162℃。 元素分析値:C19H13BrN2O分子量365.22とし
て C H N 計算値(%) 62.49 3.59 7.67 実測値(%) 62.43 3.61 7.65 このようにして得られた本発明化合物を第1表
に示す。 但し、第1表の化合物が本発明化合物を限定す
るものではない。 なお、表中の化合物番号は、試験例、製剤例に
於いても適用される。
The present invention is based on the general formula [] (In the formula, X represents a hydrogen atom or a halogen atom, Y represents a halogen atom, and m represents an integer of 0 to 2.) A 4H-3,1-benzoxazine derivative represented by The present invention relates to an agricultural and horticultural fungicide characterized by containing one or more of these 4H-3,1-benzoxazine derivatives. Many synthetic organic compounds and antibiotics with bactericidal properties have already been discovered, and many substances have been developed as fungicides for agriculture and horticulture. However, in recent years, the emergence of resistant bacteria and environmental pollution due to mass spraying have become problems. In addition, in recent years, many inventions related to so-called azole compounds as agricultural and horticultural fungicides have been announced.
For example, JP-A-56-152446, JP-A-57-16870, JP-A-57-48982, JP-A-57-120579, JP-A-57-
There are 126479. However, these compounds often have plant growth-inhibiting and herbicidal effects, and have the drawback that they cannot necessarily be said to be safe to use. In order to compensate for these drawbacks, the present inventors have worked diligently to develop a drug that has a novel skeleton and is highly effective even in small amounts, and have completed the present invention. The compound of the present invention represented by the general formula does not show any adverse effects. The compound of the present invention represented by the general formula [] is widely applicable as an agricultural and horticultural fungicide for both prevention and treatment against various pathogenic bacteria belonging to the fungi, ascomycetes, basidiomycetes, and deuteromycetes. You can. In particular, it shows excellent efficacy against powdery mildew, rust, etc. of useful plants. The compound of the present invention represented by the general formula [] (However, in the formula, X represents a hydrogen atom or a halogen atom, Y represents a halogen atom, and m represents an integer of 0 to 2.) It can be produced by ring-closing the aminobenzhydrol derivative represented by I can do it. The aminobenzhydrol derivative represented by the general formula [] is known, for example, from JP-A-57-59867. The aminobenzhydrol derivative represented by the general formula [] is ring-closed by using a so-called halogenating agent, such as thionyl chloride, thionyl bromide, phosphorus trichloride, phosphorus tribromide, phosphorus pentachloride, etc., to form 4H- 3,1-benzoxazine derivative []
can be manufactured. In order to carry out this ring-closing reaction with good yield, it is more preferable to use a deoxidizing agent such as pyridine, triethylamine, dialkylamine, or the like. Furthermore, an appropriate solvent may be used to allow the reaction to proceed smoothly. All of the deoxidizing agents mentioned above are liquids, and it is natural that they can act as a solvent as well as acting as a solvent if used in excess. For example, benzene, toluene, chloroform, etc. can be used as a material that gives a . Although room temperature is sufficient without requiring any special operation, the reaction temperature is generally -5°C to 30°C, preferably 0°C to 20°C. Next, a manufacturing example will be shown and explained. In addition, the position indication (numbering) of the bone nucleus of the compound of the present invention [] is as follows. Production example 1 4-(4'-chlorophenyl)-2-(4-pyridyl)-4H-3,1-benzoxazine (compound number 4) 2-(4-chloro-α) was added to 200 ml of pyridine under ice cooling.
-hydroxybenzyl)-isonicotine anilide
11.3 g was added thereto, and further 4 g of thionyl chloride was gradually added and stirred for 1 hour. After the reaction was further stirred at room temperature, the reaction mixture was poured into water to precipitate crystals. The obtained crystals were separated, dissolved in ethyl acetate, washed with water, and the ethyl acetate solution was dried over anhydrous awn crystals. Separate the anhydrous awn crystals and distill off the acetic acid ethyl ester under reduced pressure.
Recrystallization from a mixed solvent of n-hexane gave 9.8 g (yield: 92%) of the desired product. Melting point 116-117℃. Elemental analysis value: C 19 H 13 ClN 2 O molecular weight 320.77 C H N Calculated value (%) 71.14 4.08 8.73 Actual value (%) 71.19 4.01 8.70 Production example 2 4-(4'-chlorophenyl)-6-fluoro-2
-(4-pyridyl)-4H-3,1-benzoxazine (compound number 11) 2-(4-chloro-α-hydroxybenzyl)-
Using 11.9 g of 4-fluoro-isonicotine anilide, the same procedure as in Production Example 1 was carried out to obtain 10.2 g of the desired product (yield: 90
%) was obtained. Melting point 144-145℃. Elemental analysis value: C 19 H 12 ClFN 2 O molecular weight 338.77 C H N Calculated value (%) 67.36 3.57 8.27 Actual value (%) 67.31 3.62 8.23 Production example 3 6-chloro-4-(4'-chlorophenyl)-2 −
(4-pyridyl)-4H-3,1-benzoxazine (compound number 8) 4-chloro-2-(4-
12.4 g of chloro-α-hydroxybenzyl)-isonicotine anilide and 5.0 ml of triethylamine were dissolved, and 9.1 g of phosphorus tribromide was gradually added under ice-cooling and stirring, followed by continued stirring for 1 hour. After further stirring for 3 hours at room temperature, the reaction mixture is poured into water.
The chloroform layer was thoroughly washed with water and then dried. After chloroform was completely distilled off under reduced pressure, the product was recrystallized from a mixed solvent of ethyl acetate and n-hexane to obtain 10.1 g (yield: 85%) of the desired product. Melting point 140~
141℃. Elemental analysis value: C 19 H 12 Cl 2 N 2 O molecular weight 352.23 C H N Calculated value (%) 64.24 3.41 7.89 Actual value (%) 64.29 3.38 7.91 Production example 4 6-bromo-4-phenyl-2-(4 -pyridyl)-4H-3,1-benzoxazine (compound number 3) 4-bromo-2-(α
-hydroxybenzyl)-isonicotine anilide
Using 12.8g, react with 6.0ml of diethylaniline instead of triethylamine to obtain the desired product.
10.3g (85% yield) was obtained. Melting point 161-162℃. Elemental analysis value: C 19 H 13 BrN 2 O molecular weight 365.22 C H N Calculated value (%) 62.49 3.59 7.67 Actual value (%) 62.43 3.61 7.65 The compounds of the present invention thus obtained are shown in Table 1. However, the compounds in Table 1 do not limit the compounds of the present invention. In addition, the compound numbers in the table are also applied to test examples and formulation examples.

【表】 このようにして得られた本発明化合物は、植物
に対し浸透移行性を有するので処理方法として
は、地上部茎葉処理、種子処理、水面処理あるい
は土壌処理等あらゆる処理方法が可能である。 又、本発明化合物は対象とする有用植物に対し
てなんら悪影響を及ぼさないため、本発明化合物
の使用時期は、有用植物の播種前、播種期、幼苗
期、生育期又は結実期等あらゆる段階での使用が
可能である。 本発明化合物を実際に使用するに当つては、他
成分を加えずにそのまま使用することも可能であ
るが、より便利に使用出来るように一般の農薬の
調剤に用いられる固体、液体の各種担体と混合し
て、水和剤、乳剤、油剤、粉剤、粒剤、フロアブ
ル剤等に製造することが出来る。さらに薬剤に分
散剤、希釈剤、乳化剤、展着剤、湿展剤、吸着
剤、増粘剤、消泡剤、凍結防止剤等の補助剤を添
加することも出来る。 ここにいう担体とは、固体、液体のいずれでも
よく、またこれらの組合せでもよい。これらの例
を列記すれば、タルク、クレー、ベントナイト、
カオリン、珪そう土、炭酸カルシウム、木粉、澱
粉、アラビアゴム、水、アルコール、ケロシン、
ナフサ、キシレン、シクロヘキサノン、メチルナ
フタレン、ベンゼン、アセトン、ジメチルホルム
アミド、グリコールエーテル、N−メチルピロリ
ドン等があげられる。 補助剤としては、例えばポリオキシエチレンア
ルキルフエニールエーテル、ポリオキシエチレン
ソルビタンモノオレエート、エチレンオキシドプ
ロピレンオキシド共重合体、リグニンスルホン酸
塩、ソルビタンエステル、石けん類、硫酸化油
類、アルキル硫酸エステル塩類、石油スルホネー
ト類、ジオクチルスルホサクシネート塩類、アル
キルベンゼンスルホン酸塩、脂肪族アミン塩類、
第4級アンモニウム塩類、アルキルピリジニウム
塩類、アルキルアミノエチルグリシン、アルキル
ジメチルベタイン、ポリグリコール硫酸エステ
ル、アルキルアミンスルホン酸、リン酸イソプロ
ピル、カルボキシメチルセルロース、ポリビニー
ルアルコール、ヒドロキシプロピルセルローズ、
エチレングリコール、キサンタンガム等があげら
れる。 又、フルオロトリクロロメタン、ジクロロジフ
ルオロメタン等の噴霧剤と混合することによりエ
アゾール剤として使用したり、適当な発泡剤、燃
焼剤と混合することにより燻蒸剤または燻煙剤と
して使用することも出来る。 製剤化に当り、混合比率は一般的には本発明化
合物を重量%として、0.05〜95%好ましくは0.1
〜80%、特に好ましくは1〜70%を含有し、担体
として70〜99%、補助剤として0〜20%が最適で
ある。又、他の殺菌剤或いは除草剤、植物生長調
節剤、殺虫剤、殺ダニ剤等の農薬や肥料等と混合
して使用することにより、より広範囲な効果を期
待することが出来る。 本発明化合物を実際に使用するに際しては、使
用時期、気象条件、使用方法、使用剤型、使用場
所、対象病害、対象作物等によつて適宜選択され
ることは当然であるが、使用濃度は一般的には
0.5〜1000ppm、好ましくは3〜500ppmであり、使用
薬量(本発明化合物として)一般的には10アール
当り0.5〜500g、好ましくは10アール当り1〜
250gである。 次に試験例により本発明化合物の農園芸用殺菌
剤としての有用性を説明する。 試験例 1 キユウリうどんこ病防除試験(予防効果) 径15cmの素焼鉢に園芸用粒状培土をつめ、キユ
ウリ(品種:高砂)10粒を播種した。これを温室
内で10日間栽培し、子葉が展開した幼苗を供試し
た。 此の幼苗に製剤例2により得られた本発明化合
物の水和剤を水で所定濃度に希釈し、1鉢当り15
mlを噴霧散布した。薬液風乾後、キユウリうどん
こ病菌(Sphaerotheca fuliginea)の分生胞子水
溶液を茎葉部に噴霧接種した。接種後、23〜26℃
の温室条件下で10日間栽培したのち発病状態を調
査した。 発病度は下記の方法により算出した。 すなわち、調査葉の病斑面積に応じて、下記の
如く0,1,2,3,4,5の発病程度指数に分
類した。
[Table] Since the compound of the present invention thus obtained has systemic transferability to plants, any treatment method is possible, such as above-ground foliage treatment, seed treatment, water surface treatment, or soil treatment. . In addition, since the compounds of the present invention do not have any adverse effects on the target useful plants, the compounds of the present invention can be used at any stage of the useful plants, including before sowing, during the sowing period, during the seedling stage, during the growing season, and during the fruiting stage. It is possible to use When actually using the compound of the present invention, it is possible to use it as it is without adding other ingredients, but in order to make it more convenient to use, various solid and liquid carriers that are used in the preparation of general agricultural chemicals can be used. It can be mixed with powders to produce wettable powders, emulsions, oils, powders, granules, flowables, etc. Furthermore, auxiliary agents such as dispersants, diluents, emulsifiers, spreading agents, wetting agents, adsorbents, thickeners, antifoaming agents, and antifreezing agents can be added to the drug. The carrier referred to herein may be either solid or liquid, or a combination thereof. Examples of these include talc, clay, bentonite,
Kaolin, diatomaceous earth, calcium carbonate, wood flour, starch, gum arabic, water, alcohol, kerosene,
Examples include naphtha, xylene, cyclohexanone, methylnaphthalene, benzene, acetone, dimethylformamide, glycol ether, and N-methylpyrrolidone. Examples of adjuvants include polyoxyethylene alkyl phenyl ether, polyoxyethylene sorbitan monooleate, ethylene oxide propylene oxide copolymer, lignin sulfonate, sorbitan ester, soaps, sulfated oils, alkyl sulfate ester salts, Petroleum sulfonates, dioctyl sulfosuccinate salts, alkylbenzene sulfonates, aliphatic amine salts,
Quaternary ammonium salts, alkylpyridinium salts, alkylaminoethylglycine, alkyldimethylbetaine, polyglycol sulfate, alkylamine sulfonic acid, isopropyl phosphate, carboxymethyl cellulose, polyvinyl alcohol, hydroxypropyl cellulose,
Examples include ethylene glycol and xanthan gum. It can also be used as an aerosol agent by mixing with a propellant such as fluorotrichloromethane or dichlorodifluoromethane, or as a fumigant or smoke agent by mixing with an appropriate blowing agent or combustion agent. In formulation, the mixing ratio is generally 0.05 to 95%, preferably 0.1% by weight of the compound of the present invention.
~80%, particularly preferably 1~70%, optimally 70~99% as a carrier and 0~20% as an adjuvant. Furthermore, by mixing with other fungicides, herbicides, plant growth regulators, insecticides, acaricides, and other pesticides, fertilizers, etc., a wider range of effects can be expected. When actually using the compound of the present invention, it is natural that the concentration should be selected appropriately depending on the time of use, weather conditions, method of use, dosage form, place of use, target disease, target crop, etc. In general
The amount is 0.5 to 1000 ppm, preferably 3 to 500 ppm, and the amount used (as the compound of the present invention) is generally 0.5 to 500 g per 10 are, preferably 1 to 1 to 500 g per 10 are.
It is 250g. Next, the usefulness of the compound of the present invention as a fungicide for agriculture and horticulture will be explained using test examples. Test Example 1 Powdery mildew control test on cucumber (preventive effect) A clay pot with a diameter of 15 cm was filled with granular soil for horticulture, and 10 seeds of cucumber (variety: Takasago) were sown. This was cultivated in a greenhouse for 10 days, and the young seedlings with expanded cotyledons were used as samples. The hydrating powder of the compound of the present invention obtained in Formulation Example 2 was diluted with water to a predetermined concentration on these young seedlings, and 15% of the powder was added per pot.
ml was sprayed. After the chemical solution was air-dried, a conidial aqueous solution of Sphaerotheca fuliginea was spray inoculated onto the shoots and leaves. After inoculation, 23-26℃
After cultivating for 10 days under greenhouse conditions, the disease state was investigated. The disease severity was calculated by the following method. That is, the lesions were classified into disease severity indexes of 0, 1, 2, 3, 4, and 5 as shown below, depending on the lesion area of the investigated leaves.

【表】 かくして得られた発病程度指数をもとに下式に
より発病度を算出し、さらに無処理区の発病度と
の比較から下式により防除価を算出した。 発病度(%) =Σ(発病程度指数)×(調査葉数)/5×(調査葉数
)×100 防除価(%) =(無処理区発病度)−(処理区発病度)/(無処理区
発病度) ×100 その結果を第2表に示す。
[Table] Based on the disease severity index thus obtained, the disease severity was calculated using the formula below, and the control value was further calculated from the comparison with the disease severity in the untreated area using the formula below. Disease severity (%) = Σ ( disease severity index ) × ( number of investigated leaves ) / 5 × ( number of investigated leaves ) × 100 Control value ( % ) = ( disease severity in untreated area ) - ( disease severity in treated area ) / ( Disease severity in untreated plot) ×100 The results are shown in Table 2.

【表】 試験例 2 キユウリうどんこ病防除試験(治療効果) 径15cmの素焼鉢に園芸用培土をつめ、キユウリ
(品種:高砂)10粒を播種し、温室内で10日間栽
培し、子葉が完全展開した幼苗を供試した。この
幼苗にキユウリうどんこ病菌(Sphaerotheca
fuliginea)の分生胞子水溶液を噴霧接種し、23
〜26℃の温室内に1日放置後、製剤例3により得
られた本発明化合物の乳剤を水で所定濃度に希釈
し、1鉢当り15ml噴霧散布した。風乾後、23〜26
℃の温室条件下で10日間栽培した後、発病状態を
調査した。 発病状態指数、発病度および防除価は試験例1
に準ずる。 その結果を第3表に示す。
[Table] Test example 2 Powdery mildew control test on cucumber (therapeutic effect) A clay pot with a diameter of 15 cm was filled with horticultural soil, 10 seeds of cucumber (variety: Takasago) were sown, and the seeds were cultivated in a greenhouse for 10 days until the cotyledons grew. Fully expanded young seedlings were tested. This young seedling is infected with the powdery mildew fungus (Sphaerotheca).
fuliginea) was spray inoculated with an aqueous solution of conidia.
After being left in a greenhouse at ~26°C for one day, the emulsion of the compound of the present invention obtained in Formulation Example 3 was diluted with water to a predetermined concentration and sprayed at 15 ml per pot. After air drying, 23-26
After cultivation for 10 days under greenhouse conditions at ℃, the disease state was investigated. The disease state index, disease severity, and control value are as in Test Example 1.
According to. The results are shown in Table 3.

【表】 試験例 3 小麦うどんこ病防除試験(予防効果) 径12cmの素焼鉢に荒木田土壌をつめ、小麦(品
種:農林61号)15粒を播種した。これを温室内で
12日間栽培し第1葉が展開した幼苗を供試した。 この幼苗に製剤例4の方法で得られた本発明化
合物の乳剤を水で所定濃度に希釈し1鉢当り15ml
を噴霧散布した。 風乾後、小麦うどんこ病菌(Erysiphe
graminis)の分生胞子水溶液を噴霧接種した。
接種後20〜24℃の温度条件下10日間栽培したのち
発病状態を調査した。 発病程度指数、発病度および防除価は試験例1
に準ずる。 その結果を第4表に示す。
[Table] Test Example 3 Wheat powdery mildew control test (preventive effect) A clay pot with a diameter of 12 cm was filled with Arakida soil, and 15 grains of wheat (variety: Norin No. 61) were sown. Do this in a greenhouse
Seedlings that had been cultivated for 12 days and had developed their first leaves were used as samples. The emulsion of the compound of the present invention obtained by the method of Formulation Example 4 was diluted with water to a predetermined concentration on the seedlings, and 15 ml was added to each pot.
was sprayed. After air drying, wheat powdery mildew (Erysiphe
graminis) was inoculated by spraying with an aqueous solution of conidia.
After inoculation, the plants were cultivated for 10 days at a temperature of 20 to 24°C, and then the disease state was investigated. The disease severity index, disease severity, and control value are as in Test Example 1.
According to. The results are shown in Table 4.

【表】 試験例 4 小麦うどんこ病防除試験(治療効果) 径12cmの素焼鉢に荒木田土壌をつめ、小麦(品
種:農林61号)15粒を播種し、12日間温室内で栽
培し第1葉が展開した幼苗を供試した。 この幼苗に小麦うどんこ病菌(Erysiphe
graminis)の分生胞子水溶液を噴霧接種し、接
種後20〜23℃の温度条件下に1日放置後、製剤例
2の方法で得られた本発明化合物の水和剤を水で
所定濃度に希釈し、1鉢当り15mlを噴霧散布し、
風乾後20〜24℃の温室内で10日間栽培したのち発
病状態を調査した。 発病程度指数、発病度および防除価は試験例1
に準ずる。その結果を第5表に示す。
[Table] Test example 4 Wheat powdery mildew control test (therapeutic effect) Fill a clay pot with a diameter of 12 cm with Arakida soil, sow 15 grains of wheat (variety: Norin No. 61), and cultivate it in a greenhouse for 12 days. Young seedlings with expanded leaves were tested. This young seedling is infected with wheat powdery mildew fungus (Erysiphe).
After inoculation by spraying with an aqueous solution of conidia of P. graminis and leaving it for 1 day at a temperature of 20 to 23°C, add a wettable powder of the compound of the present invention obtained by the method of Formulation Example 2 to a predetermined concentration with water. Dilute and spray 15ml per pot.
After air-drying, the plants were cultivated in a greenhouse at 20-24°C for 10 days, and then the disease state was investigated. The disease severity index, disease severity, and control value are as in Test Example 1.
According to. The results are shown in Table 5.

【表】 以下に製剤例を示す。例中「部」は「重量部」
を示す。 製剤例1 粉剤 化合物番号8 2部 クレー 98部 以上を混合し、微粉砕して粉剤を得る。 製剤例2 水和剤 化合物番号2 10部 アルキルスルホン酸ソーダ 5部 クレー 85部 以上を混合し、微粉砕して水和剤を得る。 製剤例3 乳剤 化合物番号4 5部 アルキルベンゼンスルホン酸カルシウム 4部 ポリオキシエチレンアルキルフエニールエーテル
11部 シクロヘキサノン 10部 キシレン 70部 以上を混合して乳剤を得る。 製剤例4 乳剤 化合物番号12 10部 アルキルベンゼンスルホン酸カルシウム 3部 ポリオキシエチレンアルキルフエニルエーテル
12部 ジメチルホルムアミド 10部 キシレン 65部 以上を混合して乳剤を得る。 製剤例5 粒剤 化合物番号1 2部 リグニンスルホン酸カルシウム 2部 ベントナイト 30部 タルク 66部 以上を混合し、水を加えて練合したのち造粒し
乾燥して粒剤を得る。 製剤例6 フロアブル剤 化合物番号4 10部 エチレングリコール 5部 キサンタンガム 0.2部 ポリオキシエチレンソルビタンモノオレエート
5部 水 79.8部 以上を湿式粉砕してフロアブル製剤を得る。
[Table] Examples of formulations are shown below. "Parts" in the examples are "parts by weight"
shows. Formulation Example 1 Powder Compound No. 8 2 parts Clay 98 parts The above ingredients are mixed and pulverized to obtain a powder. Formulation Example 2 Wettable powder Compound No. 2 10 parts Sodium alkylsulfonate 5 parts Clay 85 parts The above ingredients are mixed and pulverized to obtain a wettable powder. Formulation Example 3 Emulsion Compound No. 4 5 parts Calcium alkylbenzenesulfonate 4 parts Polyoxyethylene alkyl phenyl ether
Mix 11 parts cyclohexanone 10 parts xylene 70 parts to obtain an emulsion. Formulation Example 4 Emulsion Compound No. 12 10 parts Calcium alkylbenzenesulfonate 3 parts Polyoxyethylene alkyl phenyl ether
12 parts dimethylformamide 10 parts xylene 65 parts Mix the above to obtain an emulsion. Formulation Example 5 Granules Compound No. 1 2 parts Calcium ligninsulfonate 2 parts Bentonite 30 parts Talc 66 parts The above ingredients are mixed, water is added, kneaded, granulated, and dried to obtain granules. Formulation example 6 Flowable agent Compound number 4 10 parts Ethylene glycol 5 parts Xanthan gum 0.2 parts Polyoxyethylene sorbitan monooleate
5 parts Water 79.8 parts Wet grind the above to obtain a flowable formulation.

Claims (1)

【特許請求の範囲】 1 一般式 (但し、式中、Xは水素原子又はハロゲン原子
を示し、Yはハロゲン原子を示し、mは0〜2の
整数を示す。) で表わされる4H−3,1−ベンゾオキサジン誘
導体。 2 一般式 (但し式中、Xは水素原子又はハロゲン原子を
示し、Yはハロゲン原子を示し、mは0〜2の整
数を示す。) で表わされるアミノベンズヒドロール誘導体を閉
環させることを特徴とする一般式 (但し式中、Xは水素原子又はハロゲン原子を
示し、Yはハロゲン原子を示し、mは0〜2の整
数を示す。) で表わされる4H−3,1−ベンゾオキサジン誘
導体の製造法。 3 一般式 (但し式中、Xは水素原子又はハロゲン原子を
示し、Yはハロゲン原子を示し、mは0〜2の整
数を示す。) で表わされる4H−3,1−ベンゾオキサジン誘
導体の1種又は2種以上を含有することを特徴と
する農園芸用殺菌剤。
[Claims] 1. General formula (However, in the formula, X represents a hydrogen atom or a halogen atom, Y represents a halogen atom, and m represents an integer of 0 to 2.) 4H-3,1-benzoxazine derivative represented by: 2 General formula (However, in the formula, X represents a hydrogen atom or a halogen atom, Y represents a halogen atom, and m represents an integer of 0 to 2.) A general product characterized by ring-closing an aminobenzhydrol derivative represented by formula (However, in the formula, X represents a hydrogen atom or a halogen atom, Y represents a halogen atom, and m represents an integer of 0 to 2.) A method for producing a 4H-3,1-benzoxazine derivative represented by the formula: 3 General formula (However, in the formula, X represents a hydrogen atom or a halogen atom, Y represents a halogen atom, and m represents an integer of 0 to 2.) One or two of the 4H-3,1-benzoxazine derivatives represented by An agricultural and horticultural fungicide characterized by containing seeds or more.
JP4796783A 1983-03-24 1983-03-24 4h-3,1-benzoxazine derivative, its preparation and agricultural and horticultural fungicide containing it Granted JPS59175489A (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
JP4796783A JPS59175489A (en) 1983-03-24 1983-03-24 4h-3,1-benzoxazine derivative, its preparation and agricultural and horticultural fungicide containing it
US06/589,018 US4596801A (en) 1983-03-24 1984-03-13 4H-3,1-benzoxazine derivatives, process for producing the same and agricultural or horticultural fungicide containing the same
CA000449586A CA1228590A (en) 1983-03-24 1984-03-14 4h-3,1-benzoxazine derivatives, process for producing the same and agricultural or horticultural fungicide containing the same
AU25806/84A AU562226B2 (en) 1983-03-24 1984-03-16 Pyridyl-benzoxazines
AT84103191T ATE28198T1 (en) 1983-03-24 1984-03-22 4H-3,1 BENZOXAZINE DERIVATIVES, PROCESS FOR THEIR MANUFACTURE AND ANTI-FUNGI AGRICULTURAL OR HORTICULTURAL PRODUCT CONTAINING THEM.
DE8484103191T DE3464608D1 (en) 1983-03-24 1984-03-22 4h-3,1-benzoxazine derivatives, process for producing the same and agricultural or horticultural fungicide containing the same
EP84103191A EP0120480B1 (en) 1983-03-24 1984-03-22 4h-3,1-benzoxazine derivatives, process for producing the same and agricultural or horticultural fungicide containing the same
ES530959A ES8604947A1 (en) 1983-03-24 1984-03-23 A DERIVATIVE OF 4H-3, 1-BENZOXAZINE
BR8401360A BR8401360A (en) 1983-03-24 1984-03-23 4H-3,1-BENZOXAZINE DERIVATIVE, PROCESS FOR THE PRODUCTION OF THE SAME, AGRICULTURAL OR HORTICOLA FUNGICIDE COMPOSITION AND PROCESS FOR CONTROL OF PATHOGENIC FUNGI IN PLANTS OR SOIL
ES544241A ES8604194A1 (en) 1983-03-24 1985-06-14 A PROCEDURE TO PRODUCE A DERIVATIVE OF 4H-3,1-BENZO- XAZINA

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4796783A JPS59175489A (en) 1983-03-24 1983-03-24 4h-3,1-benzoxazine derivative, its preparation and agricultural and horticultural fungicide containing it

Publications (2)

Publication Number Publication Date
JPS59175489A JPS59175489A (en) 1984-10-04
JPH0123472B2 true JPH0123472B2 (en) 1989-05-02

Family

ID=12790094

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4796783A Granted JPS59175489A (en) 1983-03-24 1983-03-24 4h-3,1-benzoxazine derivative, its preparation and agricultural and horticultural fungicide containing it

Country Status (1)

Country Link
JP (1) JPS59175489A (en)

Also Published As

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