4-(5-(3-(5H-pyrrolo[3,2-d]pyrimidin-4-yl)pyridin-2-ylamino)-6-methylisoquinolin-1-ylamino)benzonitrile

Base Information

Chemical Name:4-(5-(3-(5H-pyrrolo[3,2-d]pyrimidin-4-yl)pyridin-2-ylamino)-6-methylisoquinolin-1-ylamino)benzonitrile
CAS No.:1093100-22-1
Molecular Formula:C₂₈H₂₀N₈
Molecular Weight:468.52
Hs Code.:

Synonyms:4-(5-(3-(5H-pyrrolo[3,2-d]pyrimidin-4-yl)pyridin-2-ylamino)-6-methylisoquinolin-1-ylamino)benzonitrile

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Chemical Property of 4-(5-(3-(5H-pyrrolo[3,2-d]pyrimidin-4-yl)pyridin-2-ylamino)-6-methylisoquinolin-1-ylamino)benzonitrile

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Technology Process of 4-(5-(3-(5H-pyrrolo[3,2-d]pyrimidin-4-yl)pyridin-2-ylamino)-6-methylisoquinolin-1-ylamino)benzonitrile

There total 7 articles about 4-(5-(3-(5H-pyrrolo[3,2-d]pyrimidin-4-yl)pyridin-2-ylamino)-6-methylisoquinolin-1-ylamino)benzonitrile 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:

: 1093101-55-3
4-(2-fluoropyridin-3-yl)-5H-pyrrolo[3,2-d]pyrimidine

: 1093101-46-2
4-(5-amino-6-methylisoquinolin-1-ylamino)benzonitrile

: 1093100-22-1
4-(5-(3-(5H-pyrrolo[3,2-d]pyrimidin-4-yl)pyridin-2-ylamino)-6-methylisoquinolin-1-ylamino)benzonitrile

Guidance literature:: With lithium hexamethyldisilazane; In tetrahydrofuran; at 20 ℃; for 1h;

Reference yield:

: 84905-80-6
4-Chloro-5H-pyrrolo[3,2-d]pyrimidine

: 174669-73-9
(2-fluoro-pyridin-3-yl)boronic acid

: 1093100-22-1
4-(5-(3-(5H-pyrrolo[3,2-d]pyrimidin-4-yl)pyridin-2-ylamino)-6-methylisoquinolin-1-ylamino)benzonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: potassium acetate / bis[di-t-butyl(p-dimethylaminophenyl)phosphino]palladium (II) Dichloride / water; butan-1-ol / 1 h / 100 °C

2: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / 20 °C

With potassium acetate; lithium hexamethyldisilazane; bis[di-t-butyl(p-dimethylaminophenyl)phosphino]palladium (II) Dichloride; In tetrahydrofuran; water; butan-1-ol; 1: Suzuki Coupling;

Reference yield:

: 42398-73-2,34528-67-1
6-methylisoquinoline

: 1093100-22-1
4-(5-(3-(5H-pyrrolo[3,2-d]pyrimidin-4-yl)pyridin-2-ylamino)-6-methylisoquinolin-1-ylamino)benzonitrile

Guidance literature:: Multi-step reaction with 6 steps

1.1: sulfuric acid; potassium nitrate / 1.5 h / 0 °C

2.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 4 h / 0 °C

3.1: trichlorophosphate / 1,2-dichloro-ethane / 3 h / 70 °C

4.1: isopropyl alcohol / 22 °C

4.2: 17 h / 80 °C

5.1: tin(ll) chloride / ethanol / 17 h / 70 °C

6.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / 20 °C

With sulfuric acid; potassium nitrate; 3-chloro-benzenecarboperoxoic acid; tin(ll) chloride; lithium hexamethyldisilazane; trichlorophosphate; In tetrahydrofuran; ethanol; dichloromethane; 1,2-dichloro-ethane; isopropyl alcohol;