3-Amino-4-methyl-6-phenyl-furo<2,3-b>pyridin-2-carbonsaeure-(N,N-diethyl)amid

Base Information

Chemical Name:3-Amino-4-methyl-6-phenyl-furo<2,3-b>pyridin-2-carbonsaeure-(N,N-diethyl)amid
CAS No.:150905-48-9
Molecular Formula:C₁₉H₂₁N₃O₂
Molecular Weight:323.395
Hs Code.:

Synonyms:3-Amino-4-methyl-6-phenyl-furo<2,3-b>pyridin-2-carbonsaeure-(N,N-diethyl)amid

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Chemical Property of 3-Amino-4-methyl-6-phenyl-furo<2,3-b>pyridin-2-carbonsaeure-(N,N-diethyl)amid

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Technology Process of 3-Amino-4-methyl-6-phenyl-furo<2,3-b>pyridin-2-carbonsaeure-(N,N-diethyl)amid

There total 3 articles about 3-Amino-4-methyl-6-phenyl-furo<2,3-b>pyridin-2-carbonsaeure-(N,N-diethyl)amid 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: 78.0%

: 150905-43-4
2-(N,N-Diethylaminocarbonyl)methoxy-4-methyl-6-phenyl-pyridin-3-carbonitril

: 150905-48-9
3-Amino-4-methyl-6-phenyl-furo<2,3-b>pyridin-2-carbonsaeure-(N,N-diethyl)amid

Guidance literature:: With potassium tert-butylate; In 1,4-dioxane; for 0.166667h; Heating;

Reference yield:

: 4240-97-5
4-methyl-2-phenyl-1,2-dihydro-6-oxo-5-pyridine-carbonitrile

: 150905-48-9
3-Amino-4-methyl-6-phenyl-furo<2,3-b>pyridin-2-carbonsaeure-(N,N-diethyl)amid

Guidance literature:: Multi-step reaction with 2 steps

1: 63 percent / K₂CO₃ / dimethylformamide / 2 h / 70 °C

2: 78 percent / tBuOK / dioxane / 0.17 h / Heating

With potassium tert-butylate; potassium carbonate; In 1,4-dioxane; N,N-dimethyl-formamide;

Reference yield:

: 2315-36-8
2-Chloro-N,N-diethylacetamide

: 150905-48-9
3-Amino-4-methyl-6-phenyl-furo<2,3-b>pyridin-2-carbonsaeure-(N,N-diethyl)amid

Guidance literature:: Multi-step reaction with 2 steps

1: 63 percent / K₂CO₃ / dimethylformamide / 2 h / 70 °C

2: 78 percent / tBuOK / dioxane / 0.17 h / Heating

With potassium tert-butylate; potassium carbonate; In 1,4-dioxane; N,N-dimethyl-formamide;