2-(2-(5-amino-2-methoxyphenylamino)-5-chloropyrimidin-4-ylamino)-N-methylbenzamide

Base Information

Chemical Name:2-(2-(5-amino-2-methoxyphenylamino)-5-chloropyrimidin-4-ylamino)-N-methylbenzamide
CAS No.:1346447-74-2
Molecular Formula:C₁₉H₁₉ClN₆O₂
Molecular Weight:398.852
Hs Code.:

Synonyms:2-(2-(5-amino-2-methoxyphenylamino)-5-chloropyrimidin-4-ylamino)-N-methylbenzamide

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Chemical Property of 2-(2-(5-amino-2-methoxyphenylamino)-5-chloropyrimidin-4-ylamino)-N-methylbenzamide

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Technology Process of 2-(2-(5-amino-2-methoxyphenylamino)-5-chloropyrimidin-4-ylamino)-N-methylbenzamide

There total 4 articles about 2-(2-(5-amino-2-methoxyphenylamino)-5-chloropyrimidin-4-ylamino)-N-methylbenzamide 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: 64.7%

: 1346447-73-1
2-(5-chloro-2-(2-methoxy-5-nitrophenylamino)pyrimidin-4-ylamino)-N-methylbenzamide

: 1346447-74-2
2-(2-(5-amino-2-methoxyphenylamino)-5-chloropyrimidin-4-ylamino)-N-methylbenzamide

Guidance literature:: With hydrogen; platinum(IV) oxide; In methanol; ethyl acetate; at 20 ℃; for 1h;

Reference yield:

: 761440-08-8
2-[(2,5-dichloropyrimidin-4-yl)amino]-N-methyl-benzamide

: 1346447-74-2
2-(2-(5-amino-2-methoxyphenylamino)-5-chloropyrimidin-4-ylamino)-N-methylbenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: toluene-4-sulfonic acid / isopropyl alcohol / 6 h / 80 °C

2: hydrogen / platinum(IV) oxide / ethyl acetate; methanol / 1 h / 20 °C

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

Reference yield:

: 4141-08-6
2-Amino-N-methylbenzamid

: 1346447-74-2
2-(2-(5-amino-2-methoxyphenylamino)-5-chloropyrimidin-4-ylamino)-N-methylbenzamide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / N,N-dimethyl-formamide / 1 h / 80 °C

2: toluene-4-sulfonic acid / isopropyl alcohol / 6 h / 80 °C

3: hydrogen / platinum(IV) oxide / ethyl acetate; methanol / 1 h / 20 °C

With hydrogen; potassium carbonate; toluene-4-sulfonic acid; platinum(IV) oxide; In methanol; ethyl acetate; N,N-dimethyl-formamide; isopropyl alcohol;