JPS60112767A - ２−メトキシ−６−メチルアミノピリジンの製造法 - Google Patents

２−メトキシ−６−メチルアミノピリジンの製造法

Info

Publication number
JPS60112767A
JPS60112767A JP21947783A JP21947783A JPS60112767A JP S60112767 A JPS60112767 A JP S60112767A JP 21947783 A JP21947783 A JP 21947783A JP 21947783 A JP21947783 A JP 21947783A JP S60112767 A JPS60112767 A JP S60112767A
Authority
JP
Japan
Prior art keywords
organic layer
methylaminopyridine
dihalopyridine
reaction
methanol
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.)
Granted
Application number
JP21947783A
Other languages
English (en)
Japanese (ja)
Other versions
JPS632554B2 (enrdf_load_stackoverflow
Inventor
Kenji Tsuzuki
続木　建治
Takeshi Uotani
魚谷　武
Mitsuyuki Hashihama
橋濱　充幸
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.)
Tosoh Corp
Original Assignee
Toyo Soda Manufacturing 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 Toyo Soda Manufacturing Co Ltd filed Critical Toyo Soda Manufacturing Co Ltd
Priority to JP21947783A priority Critical patent/JPS60112767A/ja
Publication of JPS60112767A publication Critical patent/JPS60112767A/ja
Publication of JPS632554B2 publication Critical patent/JPS632554B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Pyridine Compounds (AREA)
JP21947783A 1983-11-24 1983-11-24 ２−メトキシ−６−メチルアミノピリジンの製造法 Granted JPS60112767A (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21947783A JPS60112767A (ja) 1983-11-24 1983-11-24 ２−メトキシ−６−メチルアミノピリジンの製造法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21947783A JPS60112767A (ja) 1983-11-24 1983-11-24 ２−メトキシ−６−メチルアミノピリジンの製造法

Publications (2)

Publication Number Publication Date
JPS60112767A true JPS60112767A (ja) 1985-06-19
JPS632554B2 JPS632554B2 (enrdf_load_stackoverflow) 1988-01-19

Family

ID=16736045

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21947783A Granted JPS60112767A (ja) 1983-11-24 1983-11-24 ２−メトキシ−６−メチルアミノピリジンの製造法

Country Status (1)

Country Link
JP (1) JPS60112767A (enrdf_load_stackoverflow)

Also Published As

Publication number Publication date
JPS632554B2 (enrdf_load_stackoverflow) 1988-01-19

Similar Documents

Publication Publication Date Title
Essaber et al. Synthesis of new tri-and tetraheterocyclic systems: 1, 3-dipolar cycloaddition of nitrilimines on 2, 7-dimethyl-4-phenyl-3H-1, 5-benzodiazepine
WO2010124617A1 (zh) 吡唑基丙烯腈类化合物及其应用
CN113061125B (zh) 一种咪唑啉酮化合物的制备方法
US2708675A (en) Chlorotoloxy-ethyl sulfates
CN104876920A (zh) 异噁唑类化合物、中间体及其制备方法和应用
JPS60112767A (ja) ２−メトキシ−６−メチルアミノピリジンの製造法
CA1256879A (en) 2-(5,5-disubstituted-4-oxo-2-imidazolin-2-yl) pyridine compounds
CN110981813A (zh) 一种2-氰基-5-芳基-1h-咪唑类化合物的合成方法
JPH09328477A (ja) 除草性イソオキサゾリン誘導体
CN103288693B (zh) 一种制备1-巯基芘及其中间体化合物的方法
Lee et al. Synthesis of 1, 3-oxazolidines by copper-catalyzed addition of acetone and ethyl diazoacetate to imines
CN110054609A (zh) 一种恶虫威中间体及原药的制备方法
JPS63258462A (ja) ２−フエノキシピリミジン誘導体及び除草剤
JPS6013763A (ja) ２−メトキシ−６−メチルアミノピリジンの製造法
JPS632955B2 (enrdf_load_stackoverflow)
JPH01301668A (ja) マンデル酸誘導体及び除草剤
JPH01113333A (ja) ３−（４’−ブロモビフェニル−４−イル）テトラリン−１−オンの製造方法
JP2517296B2 (ja) シクロヘキサン誘導体およびそれを有効成分とする除草剤
US3959370A (en) N-acetyl l-polychlorobenzamide compounds
JPS632550B2 (enrdf_load_stackoverflow)
Rodios Fused v-triazolo-heterocycles. Synthesis of 4 hv-triazolo [1, 5-d][1, 3, 4] oxadiatines
US4015976A (en) N-acetyl L-polychlorobenzamide herbicides
JPS5877848A (ja) シクロヘキサン誘導体の製造方法
CN106220633A (zh) 一种含氯苯并吡嗪结构的1,2,4‑三唑衍生物作为杀菌剂的应用
Yang et al. Synthesis of a rare 3D copper cyanide compound based on 3-(5-(pyridin-4-yl)-1H-1, 2, 4-triazol-3-yl) pyridine via the transformation of acetonitrile to inorganic cyanide