(2-chloro-9-cyclopentyl-9H-purin-6-yl)-(2-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-benzyloxy}-phenyl)-amine

Base Information

Chemical Name:(2-chloro-9-cyclopentyl-9H-purin-6-yl)-(2-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-benzyloxy}-phenyl)-amine
CAS No.:778603-85-3
Molecular Formula:C₃₀H₃₆ClN₇O₂
Molecular Weight:562.115
Hs Code.:

(2-chloro-9-cyclopentyl-9<i>H</i>-purin-6-yl)-(2-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-benzyloxy}-phenyl)-amine

Synonyms:(2-chloro-9-cyclopentyl-9H-purin-6-yl)-(2-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-benzyloxy}-phenyl)-amine

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Chemical Property of (2-chloro-9-cyclopentyl-9H-purin-6-yl)-(2-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-benzyloxy}-phenyl)-amine

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Technology Process of (2-chloro-9-cyclopentyl-9H-purin-6-yl)-(2-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-benzyloxy}-phenyl)-amine

There total 7 articles about (2-chloro-9-cyclopentyl-9H-purin-6-yl)-(2-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-benzyloxy}-phenyl)-amine 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: 21.0%

: 109-01-3
1-methyl-piperazine

: 778603-79-5
(2-chloro-9-cyclopentyl-9H-purin-6-yl)-{2-[4-(2-chloro-ethoxy)-benzyloxy]-phenyl}-amine

: 778603-85-3
(2-chloro-9-cyclopentyl-9H-purin-6-yl)-(2-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-benzyloxy}-phenyl)-amine

Guidance literature:: at 50 ℃; for 2h;
DOI:10.1021/jm0493111

Reference yield:

: 137-43-9
Cyclopentyl bromide

: 778603-85-3
(2-chloro-9-cyclopentyl-9H-purin-6-yl)-(2-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-benzyloxy}-phenyl)-amine

Guidance literature:: Multi-step reaction with 2 steps

1: 60 percent / K₂CO₃ / dimethylformamide / 50 °C

2: 21 percent / 2 h / 50 °C

With potassium carbonate; In N,N-dimethyl-formamide;
DOI:10.1021/jm0493111

Reference yield:

: 623-05-2
(4-hydroxyphenyl)methanol

: 778603-85-3
(2-chloro-9-cyclopentyl-9H-purin-6-yl)-(2-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-benzyloxy}-phenyl)-amine

Guidance literature:: Multi-step reaction with 6 steps

1: 41 percent / K₂CO₃; KI; TBAB / acetone / 24 h / 50 °C

2: 63 percent / DEAD; Ph₃P / tetrahydrofuran / 4 h / 20 °C

3: 90 percent / H₂; PtO₂ / ethyl acetate / 3 h

4: 56 percent / pentan-1-ol / 5 h / 80 °C

5: 60 percent / K₂CO₃ / dimethylformamide / 50 °C

6: 21 percent / 2 h / 50 °C

With platinum(IV) oxide; tetrabutylammomium bromide; hydrogen; potassium carbonate; triphenylphosphine; potassium iodide; diethylazodicarboxylate; In tetrahydrofuran; pentan-1-ol; ethyl acetate; N,N-dimethyl-formamide; acetone; 2: Mitsunobu reaction;
DOI:10.1021/jm0493111