N₄-allyl-N₂-(3-(allyloxy)-4-(4-chloro-1H-imidazol-1-yl)phenyl)-7-(2,4-difluorophenyl)-6,7-dihydro-5H-cyclopenta[d]pyrimidine-2,4-diamine

Base Information

• Chemical Name: N₄-allyl-N₂-(3-(allyloxy)-4-(4-chloro-1H-imidazol-1-yl)phenyl)-7-(2,4-difluorophenyl)-6,7-dihydro-5H-cyclopenta[d]pyrimidine-2,4-diamine
• CAS No.: 1356010-31-5
• Molecular Formula: C₂₈H₂₅ClF₂N₆O
• Molecular Weight: 534.996

Synonyms:N₄-allyl-N₂-(3-(allyloxy)-4-(4-chloro-1H-imidazol-1-yl)phenyl)-7-(2,4-difluorophenyl)-6,7-dihydro-5H-cyclopenta[d]pyrimidine-2,4-diamine

Chemical Property of N₄-allyl-N₂-(3-(allyloxy)-4-(4-chloro-1H-imidazol-1-yl)phenyl)-7-(2,4-difluorophenyl)-6,7-dihydro-5H-cyclopenta[d]pyrimidine-2,4-diamine

Chemical Property:

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Technology Process of N₄-allyl-N₂-(3-(allyloxy)-4-(4-chloro-1H-imidazol-1-yl)phenyl)-7-(2,4-difluorophenyl)-6,7-dihydro-5H-cyclopenta[d]pyrimidine-2,4-diamine

There total 7 articles about N₄-allyl-N₂-(3-(allyloxy)-4-(4-chloro-1H-imidazol-1-yl)phenyl)-7-(2,4-difluorophenyl)-6,7-dihydro-5H-cyclopenta[d]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: 30.0%

4-(4-chloro-1H-imidazol-1-yl)-3-allyloxyaniline (1356009-05-6) + N-allyl-2-chloro-7-(2,4-difluorophenyl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-amine (1356009-93-2) → N4-allyl-N2-(3-(allyloxy)-4-(4-chloro-1H-imidazol-1-yl)phenyl)-7-(2,4-difluorophenyl)-6,7-dihydro-5H-cyclopenta[d]pyrimidine-2,4-diamine (1356010-31-5)

Guidance literature:

at 150 ℃; for 0.75h;

Reference yield:

2-(allyloxy)-1-chloro-4-nitrobenzene → N4-allyl-N2-(3-(allyloxy)-4-(4-chloro-1H-imidazol-1-yl)phenyl)-7-(2,4-difluorophenyl)-6,7-dihydro-5H-cyclopenta[d]pyrimidine-2,4-diamine (1356010-31-5)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium hydroxide / dimethyl sulfoxide / 20 h / 90 °C / Inert atmosphere

2: ammonium chloride; iron / methanol / 0.5 h / 65 °C

3: 0.75 h / 150 °C

With iron; ammonium chloride; potassium hydroxide; In methanol; dimethyl sulfoxide;

Reference yield:

2-chloro-5-nitroanisole (1009-36-5) → N4-allyl-N2-(3-(allyloxy)-4-(4-chloro-1H-imidazol-1-yl)phenyl)-7-(2,4-difluorophenyl)-6,7-dihydro-5H-cyclopenta[d]pyrimidine-2,4-diamine (1356010-31-5)

Guidance literature:

Multi-step reaction with 5 steps

1: boron tribromide / dichloromethane / -78 - 4 °C / Inert atmosphere

2: potassium carbonate / N,N-dimethyl-formamide / 0 - 20 °C / Inert atmosphere

3: potassium hydroxide / dimethyl sulfoxide / 20 h / 90 °C / Inert atmosphere

4: ammonium chloride; iron / methanol / 0.5 h / 65 °C

5: 0.75 h / 150 °C

With boron tribromide; iron; potassium carbonate; ammonium chloride; potassium hydroxide; In methanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;

upstream raw materials:

2-chloro-5-nitroanisole

5-nitro-2-chlorophenol

7-(2,4-difluorophenyl)-6,7-dihydro-1H-cyclopenta[d]pyrimidine-2,4(3H,5H)-dione

2,4-dichloro-7-(2,4-difluorophenyl)-6,7-dihydro-5H-cyclopenta[d]pyrimidine

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