2-(4-Fluorophenyl)-1-(2-(1-(S)-phenylethyl)amino-4-pyrimidinyl)-5-(4-tert.butoxycarbonyl-1-piperazinyl)imidazo[4,5-b]pyridine

Base Information

Chemical Name:2-(4-Fluorophenyl)-1-(2-(1-(S)-phenylethyl)amino-4-pyrimidinyl)-5-(4-tert.butoxycarbonyl-1-piperazinyl)imidazo[4,5-b]pyridine
CAS No.:337902-90-6
Molecular Formula:C₃₃H₃₅FN₈O₂
Molecular Weight:594.692
Hs Code.:

Synonyms:2-(4-Fluorophenyl)-1-(2-(1-(S)-phenylethyl)amino-4-pyrimidinyl)-5-(4-tert.butoxycarbonyl-1-piperazinyl)imidazo[4,5-b]pyridine

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Chemical Property of 2-(4-Fluorophenyl)-1-(2-(1-(S)-phenylethyl)amino-4-pyrimidinyl)-5-(4-tert.butoxycarbonyl-1-piperazinyl)imidazo[4,5-b]pyridine

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Technology Process of 2-(4-Fluorophenyl)-1-(2-(1-(S)-phenylethyl)amino-4-pyrimidinyl)-5-(4-tert.butoxycarbonyl-1-piperazinyl)imidazo[4,5-b]pyridine

There total 7 articles about 2-(4-Fluorophenyl)-1-(2-(1-(S)-phenylethyl)amino-4-pyrimidinyl)-5-(4-tert.butoxycarbonyl-1-piperazinyl)imidazo[4,5-b]pyridine 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: 35.0%

: 7631-86-9,105269-70-3,1317-48-2,13778-37-5,14464-46-1,14808-60-7,14832-85-0,15468-32-3,17679-64-0,87347-84-0,92283-58-4,99439-28-8,15723-40-7
SiO₂

: 337902-90-6
2-(4-Fluorophenyl)-1-(2-(1-(S)-phenylethyl)amino-4-pyrimidinyl)-5-(4-tert.butoxycarbonyl-1-piperazinyl)imidazo[4,5-b]pyridine

Guidance literature:

Reference yield:

: 27048-04-0
2-amino-6-chloro-3-nitropyridine

: 337902-90-6
2-(4-Fluorophenyl)-1-(2-(1-(S)-phenylethyl)amino-4-pyrimidinyl)-5-(4-tert.butoxycarbonyl-1-piperazinyl)imidazo[4,5-b]pyridine

Guidance literature:: Multi-step reaction with 7 steps

1: 75 percent / propan-2-ol / Heating

2: 85 percent / H₂ / Pd/C / ethanol

3: 55 percent / polyphosphoric acid / 130 - 150 °C

4: 70 percent / Na₂CO₃ / ethyl acetate / 2 h / 20 °C

5: 55 percent / dimethylformamide / 2 h / 155 °C

6: 65 percent / mCPBA; AcOH / CH₂Cl₂ / 0.5 h / 0 °C

7: 1 h / 120 °C

With PPA; hydrogen; sodium carbonate; acetic acid; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In ethanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1016/j.bmcl.2004.03.106

Reference yield:

: 337902-85-9
5-Nitro-6-amino-2-(4-ethoxycarbonyl-1-piperazinyl)pyridine

: 337902-90-6
2-(4-Fluorophenyl)-1-(2-(1-(S)-phenylethyl)amino-4-pyrimidinyl)-5-(4-tert.butoxycarbonyl-1-piperazinyl)imidazo[4,5-b]pyridine

Guidance literature:: Multi-step reaction with 6 steps

1: 85 percent / H₂ / Pd/C / ethanol

2: 55 percent / polyphosphoric acid / 130 - 150 °C

3: 70 percent / Na₂CO₃ / ethyl acetate / 2 h / 20 °C

4: 55 percent / dimethylformamide / 2 h / 155 °C

5: 65 percent / mCPBA; AcOH / CH₂Cl₂ / 0.5 h / 0 °C

6: 1 h / 120 °C

With PPA; hydrogen; sodium carbonate; acetic acid; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In ethanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2004.03.106