Production Method 1

52334-81-3

937602-15-8

Reaction Conditions

1.1 Solvents: N-Methyl-2-pyrrolidone ,  Water ;  3 h, rt

Reference

Preparation of harmful animal control compositions comprising condensed imidazole compounds and kasugamycin, and method for controlling harmful animal

, Japan, , ,

Production Method 2

52334-81-3

937602-15-8

Reaction Conditions

1.1 Solvents: N-Methyl-2-pyrrolidone ,  Water ;  3 h, rt

Reference

harmful animal control compositions containing condensed imidazole compounds and diclocymet, tricyclazole, fthalide, or pyroquilon

, Japan, , ,

Production Method 3

52334-81-3

937602-15-8

Reaction Conditions

1.1 Solvents: N-Methyl-2-pyrrolidone ,  Water ;  3 h, rt

Reference

Harmful animal control compositions containing condensed imidazole compounds and validamycin and method for controlling harmful animal

, Japan, , ,

Production Method 4

52334-81-3

937602-15-8

Reaction Conditions

1.1 Solvents: N-Methyl-2-pyrrolidone ,  Water ;  3 h, rt

Reference

Harmful animal control compositions containing condensed imidazole compounds and respiratory inhibitors and method for controlling harmful animal

, Japan, , ,

Production Method 5

52334-81-3

937602-15-8

Reaction Conditions

1.1 Solvents: N-Methyl-2-pyrrolidone ,  Water ;  3 h, rt

Reference

Preparation of harmful animal control compositions comprising condensed imidazole derivative and 4-oxo-4-[(2-phenylethyl)amino]butyric acid

, Japan, , ,

Production Method 6

52334-81-3

937602-15-8

Reaction Conditions

1.1 Solvents: N-Methyl-2-pyrrolidone ,  Water ;  3 h, rt

Reference

Preparation of fused benzimidazole derivatives and pest control composition containing them and method for controlling pests

, Japan, , ,

Production Method 7

52334-81-3

937602-15-8

Reaction Conditions

1.1 Solvents: N-Methyl-2-pyrrolidone ,  Water ;  3 h, rt

Reference

Harmful animal control compositions containing condensed imidazole compounds and cartap hydrochloride and method for controlling harmful animals

, World Intellectual Property Organization, , ,

Production Method 8

52334-81-3

937602-15-8

Reaction Conditions

1.1 Solvents: Acetonitrile ,  Water ;  6 h, 25 °C; 8 h, 25 °C

Reference

Method for producing triazole compound

, World Intellectual Property Organization, , ,

Production Method 9

52334-81-3

937602-15-8

Reaction Conditions

1.1 Solvents: Acetonitrile ;  overnight, 100 °C

Reference

Preparation of sulfur-containing polycyclic compound as agricultural insecticide

, China, , ,

Production Method 10

123-39-7

52334-81-3

937602-15-8

Reaction Conditions

1.1 4 h, reflux; reflux → rt
1.2 Reagents: Water ;  cooled

Reference

A simple synthesis of aminopyridines: use of amides as amine source

Kodimuthali, Arumugam; Mungara, Anitha; Prasunamba, Padala Lakshmi; Pal, Manojit, Journal of the Brazilian Chemical Society, 2010, 21(8), 1439-1445

Production Method 11

52334-81-3

937602-15-8

Reaction Conditions

1.1 Solvents: N-Methyl-2-pyrrolidone ,  Water ;  6 h, rt

Reference

Preparation of condensed heterocyclic compounds as agricultural and horticultural pesticides

, Japan, , ,

Production Method 12

52334-81-3

937602-15-8

Reaction Conditions

1.1 Solvents: N-Methyl-2-pyrrolidone ,  Water ;  3 h, rt

Reference

Preparation of fused heterocyclic compounds and use for pest control thereof

, World Intellectual Property Organization, , ,

Production Method 13

52334-81-3

937602-15-8

Reaction Conditions

1.1 Solvents: N-Methyl-2-pyrrolidone ,  Water ;  3 h, rt

Reference

Harmful animal control compositions containing condensed imidazole compounds and pencycuron and method for controlling harmful animal

, Japan, , ,

Production Method 14

52334-81-3

937602-15-8

Reaction Conditions

1.1 Solvents: N-Methyl-2-pyrrolidone ,  Water ;  3 h, rt

Reference

Harmful animal control compositions containing condensed imidazole compounds and resistance-inducing compounds and method for controlling harmful animal

, Japan, , ,

Production Method 15

52334-81-3

937602-15-8

Reaction Conditions

1.1 Solvents: N-Methyl-2-pyrrolidone ,  Water ;  3 h, rt

Reference

Preparation of pest control compositions comprising condensed imidazole derivative and pyridalyl

, Japan, , ,

Production Method 16

52334-81-3

937602-15-8

Reaction Conditions

1.1 Solvents: N-Methyl-2-pyrrolidone ,  Water ;  3 h, rt

Reference

Preparation of pest control compositions comprising condensed imidazole derivative and pyrethroid-compound

, Japan, , ,

N-Methyl-5-(trifluoromethyl)pyridin-2-amine Raw materials

• N-Methylformamide
• 2-chloro-5-(trifluoromethyl)pyridine

N-Methyl-5-(trifluoromethyl)pyridin-2-amine Preparation Products

• N-Methyl-5-(trifluoromethyl)pyridin-2-amine (937602-15-8)

• 1. Fe(iii)-mediated isomerization of α,α-diarylallylic alcohols to ketones via radical 1,2-aryl migration?
  Ziyang Deng,Changwei Chen,Sunliang Cui RSC Adv., 2016,6, 93753-93755
• 2. Estimation of activation energy for electroporation and pore growth rate in liquid crystalline and gel phases of lipid bilayers using molecular dynamics simulations?
  Amit Kumar Majhi,Subbarao Kanchi,V. Venkataraman,K. G. Ayappa,Prabal K. Maiti Soft Matter, 2015,11, 8632-8640
• 3. Fate of Sb(v) and Sb(iii) species along a gradient of pH and oxygen concentration in the Carnoulès mine waters (Southern France)
  Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
• 4. Excellent electrochemical performance of LiFe0.4Mn0.6PO4 microspheres produced using a double carbon coating process?
  Yong Ping Huang,Tao Tao,Zheng Chen,Wei Han,Ying Wu,Chunjiang Kuang,Shaoxiong Zhou,Ying Chen J. Mater. Chem. A, 2014,2, 18831-18837
• 5. Fast-Track to Research Data Management in Experimental Material Science-Setting the Ground for Research Group Level Materials Digitalization.
  LarsBanko,AlfredLudwig

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Aminopyridines and derivatives

• 74784-70-6(5-(Trifluoromethyl)pyridin-2-amine)
• 172648-55-4(3-Amino-2-(methylamino)-5-(trifluoromethyl)pyridine)
• 163620-24-4(2-(1-Methylhydrazinyl)-5-(trifluoromethyl)pyridine)
• 89810-00-4(2-PYRIDINAMINE, N-ETHYL-5-(TRIFLUOROMETHYL)-)
• 132664-25-6(2-Pyridinamine, N,N-diethyl-5-(trifluoromethyl)-)
• 207557-34-4(N1-[5-(trifluoromethyl)pyridin-2-yl]ethane-1,2-diamine)
• 1036584-14-1(N-methyl-3-(trifluoromethyl)pyridin-2-amine)
• 838867-08-6(3-{[5-(trifluoromethyl)pyridin-2-yl]amino}propan-1-ol)
• 874630-03-2(2-{5-(trifluoromethyl)pyridin-2-ylamino}ethan-1-ol)
• 884004-51-7(5-(trifluoromethyl)-2-Pyridinamine hydrochloride)