{2-amino-6-[2-(2-hydroxymethylpyrrolidin-1-ylmethyl)phenyl]quinazolin-4-yl}-(1,3-dihydroisoindol-2-yl)methanone

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Chemical Name:{2-amino-6-[2-(2-hydroxymethylpyrrolidin-1-ylmethyl)phenyl]quinazolin-4-yl}-(1,3-dihydroisoindol-2-yl)methanone
CAS No.:1367454-53-2
Molecular Formula:C₂₉H₂₉N₅O₂
Molecular Weight:479.582
Hs Code.:

Synonyms:{2-amino-6-[2-(2-hydroxymethylpyrrolidin-1-ylmethyl)phenyl]quinazolin-4-yl}-(1,3-dihydroisoindol-2-yl)methanone

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Chemical Property of {2-amino-6-[2-(2-hydroxymethylpyrrolidin-1-ylmethyl)phenyl]quinazolin-4-yl}-(1,3-dihydroisoindol-2-yl)methanone

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Technology Process of {2-amino-6-[2-(2-hydroxymethylpyrrolidin-1-ylmethyl)phenyl]quinazolin-4-yl}-(1,3-dihydroisoindol-2-yl)methanone

There total 5 articles about {2-amino-6-[2-(2-hydroxymethylpyrrolidin-1-ylmethyl)phenyl]quinazolin-4-yl}-(1,3-dihydroisoindol-2-yl)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: 29.0%

: 1101146-34-2
2-[2-amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]benzaldehyde

: 498-63-5
2-hydroxymethylpyrrolidine

: 1367454-53-2
{2-amino-6-[2-(2-hydroxymethylpyrrolidin-1-ylmethyl)phenyl]quinazolin-4-yl}-(1,3-dihydroisoindol-2-yl)methanone

Guidance literature:: 2-[2-amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]benzaldehyde; 2-hydroxymethylpyrrolidine; With acetic acid; In tetrahydrofuran; 1,2-dichloro-ethane; at 60 ℃; for 6h;

With sodium tris(acetoxy)borohydride; In tetrahydrofuran; 1,2-dichloro-ethane; at 25 ℃; for 12h;

Reference yield:

: 20780-76-1
5-iodoisatin

: 1367454-53-2
{2-amino-6-[2-(2-hydroxymethylpyrrolidin-1-ylmethyl)phenyl]quinazolin-4-yl}-(1,3-dihydroisoindol-2-yl)methanone

Guidance literature:: Multi-step reaction with 5 steps

1.1: tetrahydrofuran / 16 h / 10 - 23 °C

2.1: tetrahydrofuran / 0.5 h / 25 °C

3.1: cesium fluoride / acetonitrile / 0.33 h / 20 °C / Inert atmosphere

4.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate / ethanol; water / 0.5 h / 130 °C / Inert atmosphere

5.1: acetic acid / tetrahydrofuran; 1,2-dichloro-ethane / 6 h / 60 °C

5.2: 12 h / 25 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate; acetic acid; cesium fluoride; In tetrahydrofuran; ethanol; water; 1,2-dichloro-ethane; acetonitrile; 4.1: |Suzuki Coupling;

Reference yield:

: 1228311-56-5
tert-butyl 5-iodo-2,3-dioxo-2,3-dihydroindole-1-carboxylate

: 1367454-53-2
{2-amino-6-[2-(2-hydroxymethylpyrrolidin-1-ylmethyl)phenyl]quinazolin-4-yl}-(1,3-dihydroisoindol-2-yl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrahydrofuran / 0.5 h / 25 °C

2.1: cesium fluoride / acetonitrile / 0.33 h / 20 °C / Inert atmosphere

3.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate / ethanol; water / 0.5 h / 130 °C / Inert atmosphere

4.1: acetic acid / tetrahydrofuran; 1,2-dichloro-ethane / 6 h / 60 °C

4.2: 12 h / 25 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate; acetic acid; cesium fluoride; In tetrahydrofuran; ethanol; water; 1,2-dichloro-ethane; acetonitrile; 3.1: |Suzuki Coupling;