N₂-(5-amino-2-methoxy-4-(1-methylpiperidin-4-yl)phenyl)-5-chloro-N₄-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine

Base Information

• Chemical Name: N₂-(5-amino-2-methoxy-4-(1-methylpiperidin-4-yl)phenyl)-5-chloro-N₄-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine
• CAS No.: 1346448-20-1
• Molecular Formula: C₂₆H₃₃ClN₆O₃S
• Molecular Weight: 545.105

Synonyms:N₂-(5-amino-2-methoxy-4-(1-methylpiperidin-4-yl)phenyl)-5-chloro-N₄-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine

Chemical Property of N₂-(5-amino-2-methoxy-4-(1-methylpiperidin-4-yl)phenyl)-5-chloro-N₄-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine

Chemical Property:

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Technology Process of N₂-(5-amino-2-methoxy-4-(1-methylpiperidin-4-yl)phenyl)-5-chloro-N₄-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine

There total 6 articles about N₂-(5-amino-2-methoxy-4-(1-methylpiperidin-4-yl)phenyl)-5-chloro-N₄-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine 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: 32.0%

5-chloro-N4-(2-(isopropylsulfonyl)phenyl)-N2-(2-methoxy-4-(1-methylpiperidin-4-yl)-5-nitrophenyl)pyrimidine-2,4-diamine (1346448-19-8) → N2-(5-amino-2-methoxy-4-(1-methylpiperidin-4-yl)phenyl)-5-chloro-N4-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine (1346448-20-1)

Guidance literature:

With hydrogen; platinum(IV) oxide; In ethyl acetate; at 20 ℃; for 12h;

Reference yield:

2-methoxy-4-(1-methylpiperidin-4-yl)aniline (1124330-14-8) → N2-(5-amino-2-methoxy-4-(1-methylpiperidin-4-yl)phenyl)-5-chloro-N4-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine (1346448-20-1)

Guidance literature:

Multi-step reaction with 5 steps

1.1: water / 4 h / 20 °C

2.1: nitric acid / water / 0.5 h / 0 - 20 °C

2.2: Cooling with ice

3.1: hydrogenchloride; water / methanol / 4 h / 65 °C

4.1: toluene-4-sulfonic acid / isopropyl alcohol / 12 h / 100 °C

5.1: hydrogen / platinum(IV) oxide / ethyl acetate / 12 h / 20 °C

With hydrogenchloride; water; hydrogen; nitric acid; toluene-4-sulfonic acid; platinum(IV) oxide; In methanol; water; ethyl acetate; isopropyl alcohol;

Reference yield:

N-(2-methoxy-4-(1-methylpiperidin-4-yl)phenyl)acetamide (1346448-16-5) → N2-(5-amino-2-methoxy-4-(1-methylpiperidin-4-yl)phenyl)-5-chloro-N4-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine (1346448-20-1)

Guidance literature:

Multi-step reaction with 4 steps

1.1: nitric acid / water / 0.5 h / 0 - 20 °C

1.2: Cooling with ice

2.1: hydrogenchloride; water / methanol / 4 h / 65 °C

3.1: toluene-4-sulfonic acid / isopropyl alcohol / 12 h / 100 °C

4.1: hydrogen / platinum(IV) oxide / ethyl acetate / 12 h / 20 °C

With hydrogenchloride; water; hydrogen; nitric acid; toluene-4-sulfonic acid; platinum(IV) oxide; In methanol; water; ethyl acetate; isopropyl alcohol;

upstream raw materials:

2-methoxy-4-(1-methylpiperidin-4-yl)aniline

N-(2-methoxy-4-(1-methylpiperidin-4-yl)phenyl)acetamide

N-(2-methoxy-4-(1-methylpiperidin-4-yl)-5-nitrophenyl)acetamide

2-methoxy-4-(1-methylpiperidin-4-yl)-5-nitroaniline

Downstream raw materials:

N-(5-((5-chloro-4-((2-(isopropylsulfonyl)phenyl)amino)pyrimidin-2-yl)amino)-4-methoxy-2-(1-methylpiperidin-4-yl)phenyl)acrylamide

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