methyl 2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)oxazol-4-carboxylate

Base Information

Chemical Name:methyl 2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)oxazol-4-carboxylate
CAS No.:1328623-72-8
Molecular Formula:C₂₁H₁₇ClN₆O₄
Molecular Weight:452.857
Hs Code.:

Synonyms:methyl 2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)oxazol-4-carboxylate

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Chemical Property of methyl 2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)oxazol-4-carboxylate

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Technology Process of methyl 2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)oxazol-4-carboxylate

There total 6 articles about methyl 2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)oxazol-4-carboxylate 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: 20.0%

: 1328623-71-7
methyl 2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)-4,5-dihydrooxazol-4-carboxylate

: 1328623-72-8
methyl 2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)oxazol-4-carboxylate

Guidance literature:: With Bromotrichloromethane; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at -40 - 20 ℃; for 2.33333h;

Reference yield:

: 5305-40-8
2,6-dichloro-pyrimidine carbaldehyde

: 1328623-72-8
methyl 2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)oxazol-4-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1.1: sulfuryl dichloride / 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 1.5 h / 80 °C

2.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 0 - 20 °C

3.1: ammonia / toluene; ethanol / 60 °C

4.1: diethylamino-sulfur trifluoride / dichloromethane / -78 - 0 °C

4.2: pH 8

5.1: hydrogenchloride / 1,4-dioxane; tert-butyl alcohol / 1.5 h / 70 °C

6.1: Bromotrichloromethane; 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 2.33 h / -40 - 20 °C

With hydrogenchloride; sulfuryl dichloride; Bromotrichloromethane; diethylamino-sulfur trifluoride; ammonia; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; 2,2'-azobis(isobutyronitrile); In tetrahydrofuran; 1,4-dioxane; tetrachloromethane; ethanol; dichloromethane; toluene; tert-butyl alcohol;

Reference yield:

: 87600-97-3
4,6-dichloropyrimidine-5-carboxylic acid chloride

: 1328623-72-8
methyl 2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)oxazol-4-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 0 - 20 °C

2.1: ammonia / toluene; ethanol / 60 °C

3.1: diethylamino-sulfur trifluoride / dichloromethane / -78 - 0 °C

3.2: pH 8

4.1: hydrogenchloride / 1,4-dioxane; tert-butyl alcohol / 1.5 h / 70 °C

5.1: Bromotrichloromethane; 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 2.33 h / -40 - 20 °C

With hydrogenchloride; Bromotrichloromethane; diethylamino-sulfur trifluoride; ammonia; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; toluene; tert-butyl alcohol;