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

Base Information

Chemical Name:(2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)oxazol-4-yl)methanol
CAS No.:1364411-02-8
Molecular Formula:C₂₀H₁₇ClN₆O₃
Molecular Weight:424.846
Hs Code.:

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

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

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

There total 7 articles about (2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)oxazol-4-yl)methanol 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: 82.0%

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

: 1364411-02-8
(2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)oxazol-4-yl)methanol

Guidance literature:: methyl 2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)oxazol-4-carboxylate; With lithium aluminium tetrahydride; In diethyl ether; dichloromethane; at 0 ℃; for 1h;

With water; Rochelle's salt; In diethyl ether; dichloromethane; for 1h;

Reference yield:

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

: 1364411-02-8
(2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)oxazol-4-yl)methanol

Guidance literature:: Multi-step reaction with 7 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

7.1: lithium aluminium tetrahydride / dichloromethane; diethyl ether / 1 h / 0 °C

7.2: 1 h

With hydrogenchloride; lithium aluminium tetrahydride; 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; diethyl ether; ethanol; dichloromethane; toluene; tert-butyl alcohol;

Reference yield:

: 1328623-68-2
methyl 2-(4,6-dichloropyrimidin-5-carboxamido)-3-hydroxypropanoate

: 1364411-02-8
(2-(4-amino-6-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)pyrimidin-5-yl)oxazol-4-yl)methanol

Guidance literature:: Multi-step reaction with 5 steps

1.1: ammonia / toluene; ethanol / 60 °C

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

2.2: pH 8

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

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

5.1: lithium aluminium tetrahydride / dichloromethane; diethyl ether / 1 h / 0 °C

5.2: 1 h

With hydrogenchloride; lithium aluminium tetrahydride; Bromotrichloromethane; diethylamino-sulfur trifluoride; ammonia; 1,8-diazabicyclo[5.4.0]undec-7-ene; In 1,4-dioxane; diethyl ether; ethanol; dichloromethane; toluene; tert-butyl alcohol;