(R)-2-(2-(2,4-dimethoxybenzylamino)-4-fluorophenylamino)-9-(8-fluorochroman-4-yl)-7H-purin-8(9H)-one

Base Information

Chemical Name:(R)-2-(2-(2,4-dimethoxybenzylamino)-4-fluorophenylamino)-9-(8-fluorochroman-4-yl)-7H-purin-8(9H)-one
CAS No.:911826-26-1
Molecular Formula:C₂₉H₂₆F₂N₆O₄
Molecular Weight:560.56
Hs Code.:

Synonyms:(R)-2-(2-(2,4-dimethoxybenzylamino)-4-fluorophenylamino)-9-(8-fluorochroman-4-yl)-7H-purin-8(9H)-one

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Chemical Property of (R)-2-(2-(2,4-dimethoxybenzylamino)-4-fluorophenylamino)-9-(8-fluorochroman-4-yl)-7H-purin-8(9H)-one

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Technology Process of (R)-2-(2-(2,4-dimethoxybenzylamino)-4-fluorophenylamino)-9-(8-fluorochroman-4-yl)-7H-purin-8(9H)-one

There total 16 articles about (R)-2-(2-(2,4-dimethoxybenzylamino)-4-fluorophenylamino)-9-(8-fluorochroman-4-yl)-7H-purin-8(9H)-one 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:

: 1026790-40-8
(R)-N₂-(2-(2,4-dimethoxybenzylamino)-4-fluorophenyl)-N₄-(8-fluorochroman-4-yl)pyrimidine-2,4,5-triamine

: 530-62-1
1,1'-carbonyldiimidazole

: 911826-26-1
(R)-2-(2-(2,4-dimethoxybenzylamino)-4-fluorophenylamino)-9-(8-fluorochroman-4-yl)-7H-purin-8(9H)-one

Guidance literature:: In tetrahydrofuran; for 18h;

Reference yield:

: 911826-29-4
(R)-N-(8-fluorochroman-4-yl)-2-methoxyacetamide

: 911826-26-1
(R)-2-(2-(2,4-dimethoxybenzylamino)-4-fluorophenylamino)-9-(8-fluorochroman-4-yl)-7H-purin-8(9H)-one

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogenchloride; ethanol; water / 4 h / Heating / reflux

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 0.25 h / -78 °C

3: potassium carbonate / acetonitrile / 3 h / 65 °C

4: hydrogen / nickel / tetrahydrofuran / 2 h / 20 °C

5: tetrahydrofuran / 18 h

With hydrogenchloride; ethanol; water; hydrogen; potassium carbonate; N-ethyl-N,N-diisopropylamine; nickel; In tetrahydrofuran; acetonitrile;

Reference yield:

: 791043-28-2
8-fluorochroman-4-amine

: 911826-26-1
(R)-2-(2-(2,4-dimethoxybenzylamino)-4-fluorophenylamino)-9-(8-fluorochroman-4-yl)-7H-purin-8(9H)-one

Guidance literature:: Multi-step reaction with 6 steps

1: novozyme 435 / tert-butyl methyl ether / 2 h / Heating / reflux; Enzymatic reaction; Resolution of racemate

2: hydrogenchloride; ethanol; water / 4 h / Heating / reflux

3: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 0.25 h / -78 °C

4: potassium carbonate / acetonitrile / 3 h / 65 °C

5: hydrogen / nickel / tetrahydrofuran / 2 h / 20 °C

6: tetrahydrofuran / 18 h

With hydrogenchloride; ethanol; water; hydrogen; potassium carbonate; N-ethyl-N,N-diisopropylamine; novozyme 435; nickel; In tetrahydrofuran; tert-butyl methyl ether; acetonitrile;