4-(4-(allylamino)-7-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-2-ylamino)-2-(allyloxy)benzonitrile

Base Information

Chemical Name:4-(4-(allylamino)-7-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-2-ylamino)-2-(allyloxy)benzonitrile
CAS No.:1356010-35-9
Molecular Formula:C₂₆H₂₅N₅O
Molecular Weight:423.517
Hs Code.:

Synonyms:4-(4-(allylamino)-7-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-2-ylamino)-2-(allyloxy)benzonitrile

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Chemical Property of 4-(4-(allylamino)-7-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-2-ylamino)-2-(allyloxy)benzonitrile

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Technology Process of 4-(4-(allylamino)-7-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-2-ylamino)-2-(allyloxy)benzonitrile

There total 10 articles about 4-(4-(allylamino)-7-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-2-ylamino)-2-(allyloxy)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: 67.5%

: 757247-69-1
2-(allyloxy)-4-aminobenzonitrile

: 1356009-66-9
N-allyl-2-chloro-7-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-amine

: 1356010-35-9
4-(4-(allylamino)-7-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-2-ylamino)-2-(allyloxy)benzonitrile

Guidance literature:: at 150 ℃; for 0.75h;

Reference yield:

: 825-54-7
cyclopent-1-en-1-ylbenzene

: 1356010-35-9
4-(4-(allylamino)-7-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-2-ylamino)-2-(allyloxy)benzonitrile

Guidance literature:: Multi-step reaction with 8 steps

1.1: formic acid; dihydrogen peroxide / 4 h / 20 - 40 °C

2.1: diisopropylamine; n-butyllithium / tetrahydrofuran; hexanes / 0.5 h / -78 °C

2.2: 3 h / 25 °C

3.1: potassium hydroxide / water / 20 °C

4.1: hydrogenchloride; water / 1 h / Reflux

5.1: ammonia / water / 5 h / Heating

6.1: trichlorophosphate / 1 h / 110 °C / microwave irradiation

7.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 18 h / 20 °C

8.1: 0.75 h / 150 °C

With hydrogenchloride; n-butyllithium; formic acid; ammonia; water; dihydrogen peroxide; diisopropylamine; N-ethyl-N,N-diisopropylamine; potassium hydroxide; trichlorophosphate; In tetrahydrofuran; hexanes; water; acetonitrile;

Reference yield:

: 100-58-3
phenylmagnesium bromide

: 1356010-35-9
4-(4-(allylamino)-7-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-2-ylamino)-2-(allyloxy)benzonitrile

Guidance literature:: Multi-step reaction with 9 steps

1.1: diethyl ether; tetrahydrofuran / 2.5 h / 0 °C / Reflux

2.1: formic acid; dihydrogen peroxide / 4 h / 20 - 40 °C

3.1: diisopropylamine; n-butyllithium / tetrahydrofuran; hexanes / 0.5 h / -78 °C

3.2: 3 h / 25 °C

4.1: potassium hydroxide / water / 20 °C

5.1: hydrogenchloride; water / 1 h / Reflux

6.1: ammonia / water / 5 h / Heating

7.1: trichlorophosphate / 1 h / 110 °C / microwave irradiation

8.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 18 h / 20 °C

9.1: 0.75 h / 150 °C

With hydrogenchloride; n-butyllithium; formic acid; ammonia; water; dihydrogen peroxide; diisopropylamine; N-ethyl-N,N-diisopropylamine; potassium hydroxide; trichlorophosphate; In tetrahydrofuran; hexanes; diethyl ether; water; acetonitrile;