4-[3-[2-[4-[[(3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl]oxy]phenyl]ethyl]phenyl]pyridine

Base Information

Chemical Name:4-[3-[2-[4-[[(3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl]oxy]phenyl]ethyl]phenyl]pyridine
CAS No.:859140-04-8
Molecular Formula:C₂₈H₃₂N₂O₃
Molecular Weight:444.574
Hs Code.:

Synonyms:4-[3-[2-[4-[[(3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl]oxy]phenyl]ethyl]phenyl]pyridine

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Chemical Property of 4-[3-[2-[4-[[(3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl]oxy]phenyl]ethyl]phenyl]pyridine

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Technology Process of 4-[3-[2-[4-[[(3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl]oxy]phenyl]ethyl]phenyl]pyridine

There total 4 articles about 4-[3-[2-[4-[[(3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl]oxy]phenyl]ethyl]phenyl]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: 82.0%

: 859140-03-7
(S)-3-{4-[(E)-2-(3-Pyridin-4-yl-phenyl)-vinyl]-phenoxy}-pyrrolidine-1-carboxylic acid tert-butyl ester

: 859140-04-8
4-[3-[2-[4-[[(3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl]oxy]phenyl]ethyl]phenyl]pyridine

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; at 20 ℃; for 16h;
DOI:10.1016/j.bmc.2005.04.006

Reference yield:

: 859140-02-6
(E,Z)-3-bromo-4'-[[(3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl]oxy]stilbene

: 859140-04-8
4-[3-[2-[4-[[(3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl]oxy]phenyl]ethyl]phenyl]pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 39 percent / tetrabutylammonium bromide; potassium hydroxide / tetrakis(triphenylphosphine)palladium⁽⁰⁾ / tetrahydrofuran / 28 h / Heating

2: 82 percent / hydrogen / Pd/C / ethanol / 16 h / 20 °C

With potassium hydroxide; tetrabutylammomium bromide; hydrogen; palladium on activated charcoal; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; ethanol; 1: Suzuki-Miyaura coupling;
DOI:10.1016/j.bmc.2005.04.006

Reference yield:

: 95902-10-6
(3-bromobenzyl)(triphenyl)phosphonium bromide

: 859140-04-8
4-[3-[2-[4-[[(3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl]oxy]phenyl]ethyl]phenyl]pyridine

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / 1,8-diazabicyclo[5.4.0]-7-undecene / tetrahydrofuran; ethanol / 18 h / 20 °C

2: 39 percent / tetrabutylammonium bromide; potassium hydroxide / tetrakis(triphenylphosphine)palladium⁽⁰⁾ / tetrahydrofuran / 28 h / Heating

3: 82 percent / hydrogen / Pd/C / ethanol / 16 h / 20 °C

With potassium hydroxide; tetrabutylammomium bromide; hydrogen; 1,8-diazabicyclo[5.4.0]undec-7-ene; palladium on activated charcoal; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; ethanol; 1: Wittig reaction / 2: Suzuki-Miyaura coupling;
DOI:10.1016/j.bmc.2005.04.006