(5-methoxy-2-methyl-4-(4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)(morpholino)methanone

Base Information

Chemical Name:(5-methoxy-2-methyl-4-(4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)(morpholino)methanone
CAS No.:1401423-21-9
Molecular Formula:C₁₉H₂₂F₃N₅O₃
Molecular Weight:425.411
Hs Code.:

Synonyms:(5-methoxy-2-methyl-4-(4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)(morpholino)methanone

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Chemical Property of (5-methoxy-2-methyl-4-(4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)(morpholino)methanone

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Technology Process of (5-methoxy-2-methyl-4-(4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)(morpholino)methanone

There total 5 articles about (5-methoxy-2-methyl-4-(4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)(morpholino)methanone 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: 58.0%

: 515824-43-8
2-chloro-N-methyl-5-(trifluoromethyl)pyrimidine-4-amine

: 1401423-38-8
(4-amino-5-methoxy-2-methylphenyl)(morpholino)-methanone

: 1401423-21-9
(5-methoxy-2-methyl-4-(4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)(morpholino)methanone

Guidance literature:: With toluene-4-sulfonic acid; In 1,4-dioxane; at 100 ℃; for 18h;

Reference yield:

: 106579-00-4
5-methoxy-2-methyl-4-nitroaniline

: 1401423-21-9
(5-methoxy-2-methyl-4-(4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)(morpholino)methanone

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride; sodium nitrite / acetone; water / 0.5 h / 0 °C

1.2: 1 h / 20 °C

2.1: acetic acid; sulfuric acid / water / 5 h / 120 °C

3.1: HATU; N-ethyl-N,N-diisopropylamine / dichloromethane / 1.1 h / 20 °C

4.1: tin(II) chloride dihdyrate / ethanol; water / 5 h / 65 °C

4.2: Heating

5.1: toluene-4-sulfonic acid / 1,4-dioxane / 4 h / 100 °C

With hydrogenchloride; tin(II) chloride dihdyrate; sulfuric acid; toluene-4-sulfonic acid; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; sodium nitrite; In 1,4-dioxane; ethanol; dichloromethane; water; acetone; 1.1: |Sandmeyer Reaction / 1.2: |Sandmeyer Reaction;
DOI:10.1021/jm301020q

Reference yield:

: 1401423-35-5
(5-methoxy-2-methyl-4-nitrophenyl)(morpholino)-methanone

: 1401423-21-9
(5-methoxy-2-methyl-4-(4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)(morpholino)methanone

Guidance literature:: Multi-step reaction with 2 steps

1.1: tin(II) chloride dihdyrate / ethanol; water / 5 h / 65 °C

1.2: Heating

2.1: toluene-4-sulfonic acid / 1,4-dioxane / 4 h / 100 °C

With tin(II) chloride dihdyrate; toluene-4-sulfonic acid; In 1,4-dioxane; ethanol; water;
DOI:10.1021/jm301020q