1-methyl-3-(2-oxo-6-phenyl-4-trifluoromethyl-1,2-dihydro-pyridin-3-yl)-urea

Base Information

Chemical Name:1-methyl-3-(2-oxo-6-phenyl-4-trifluoromethyl-1,2-dihydro-pyridin-3-yl)-urea
CAS No.:216431-88-8
Molecular Formula:C₁₄H₁₂F₃N₃O₂
Molecular Weight:311.263
Hs Code.:

Synonyms:1-methyl-3-(2-oxo-6-phenyl-4-trifluoromethyl-1,2-dihydro-pyridin-3-yl)-urea

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-methyl-3-(2-oxo-6-phenyl-4-trifluoromethyl-1,2-dihydro-pyridin-3-yl)-urea

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Technology Process of 1-methyl-3-(2-oxo-6-phenyl-4-trifluoromethyl-1,2-dihydro-pyridin-3-yl)-urea

There total 1 articles about 1-methyl-3-(2-oxo-6-phenyl-4-trifluoromethyl-1,2-dihydro-pyridin-3-yl)-urea which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 86.5%

: 74-89-5
methylamine

: 179996-80-6
2-oxo-7-trifluoromethyl-5-phenyl-(1H)-oxazolo[5,4-b]pyridine

: 216431-88-8
1-methyl-3-(2-oxo-6-phenyl-4-trifluoromethyl-1,2-dihydro-pyridin-3-yl)-urea

Guidance literature:: In 1,4-dioxane; at 95 - 100 ℃; for 1.5h;
DOI:10.1007/BF02290731

Reference yield: 91.5%

: 216431-88-8
1-methyl-3-(2-oxo-6-phenyl-4-trifluoromethyl-1,2-dihydro-pyridin-3-yl)-urea

: 179996-80-6
2-oxo-7-trifluoromethyl-5-phenyl-(1H)-oxazolo[5,4-b]pyridine

Guidance literature:: With triethylamine; In N,N-dimethyl acetamide; for 3h; Heating;
DOI:10.1007/BF02290731

Reference yield:

: 216431-88-8
1-methyl-3-(2-oxo-6-phenyl-4-trifluoromethyl-1,2-dihydro-pyridin-3-yl)-urea

: 1-allyl-3-(2-oxo-6-phenyl-4-trifluoromethyl-1,2-dihydro-pyridin-3-yl)-urea

Guidance literature:: Multi-step reaction with 2 steps

1: 91.5 percent / triethylamine / N,N-dimethyl-acetamide / 3 h / Heating

2: 93.3 percent / dioxane / 2 h / 95 - 100 °C

With triethylamine; In 1,4-dioxane; N,N-dimethyl acetamide; 1: Cyclization / 2: Ring cleavage;
DOI:10.1007/BF02290731