(S)-tert-butyl 1-(2-(5-(2-(2-aminopyrimidin-5-yl)ethynyl)-2-fluorobenzamido)-4-(trifluoromethyl)phenyl)piperidin-3-yl(methyl)carbamate

Base Information

Chemical Name:(S)-tert-butyl 1-(2-(5-(2-(2-aminopyrimidin-5-yl)ethynyl)-2-fluorobenzamido)-4-(trifluoromethyl)phenyl)piperidin-3-yl(methyl)carbamate
CAS No.:884602-88-4
Molecular Formula:C₃₁H₃₂F₄N₆O₃
Molecular Weight:612.627
Hs Code.:

Synonyms:(S)-tert-butyl 1-(2-(5-(2-(2-aminopyrimidin-5-yl)ethynyl)-2-fluorobenzamido)-4-(trifluoromethyl)phenyl)piperidin-3-yl(methyl)carbamate

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Chemical Property of (S)-tert-butyl 1-(2-(5-(2-(2-aminopyrimidin-5-yl)ethynyl)-2-fluorobenzamido)-4-(trifluoromethyl)phenyl)piperidin-3-yl(methyl)carbamate

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Technology Process of (S)-tert-butyl 1-(2-(5-(2-(2-aminopyrimidin-5-yl)ethynyl)-2-fluorobenzamido)-4-(trifluoromethyl)phenyl)piperidin-3-yl(methyl)carbamate

There total 8 articles about (S)-tert-butyl 1-(2-(5-(2-(2-aminopyrimidin-5-yl)ethynyl)-2-fluorobenzamido)-4-(trifluoromethyl)phenyl)piperidin-3-yl(methyl)carbamate 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:

: 857265-74-8
5-ethynylpyrimidine-2-amine

: 884602-86-2
(S)-tert-butyl 1-(2-(2-fluoro-5-iodobenzamido)-4-(trifluoromethyl)phenyl)piperidine-3-carboxylate

: 884602-88-4
(S)-tert-butyl 1-(2-(5-(2-(2-aminopyrimidin-5-yl)ethynyl)-2-fluorobenzamido)-4-(trifluoromethyl)phenyl)piperidin-3-yl(methyl)carbamate

Guidance literature:: With triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In acetonitrile; at 70 ℃; for 16h;
DOI:10.1021/jm061112p

Reference yield:

: 186584-73-6
2-fluoro-5-iodobenzoyl chloride

: 884602-88-4
(S)-tert-butyl 1-(2-(5-(2-(2-aminopyrimidin-5-yl)ethynyl)-2-fluorobenzamido)-4-(trifluoromethyl)phenyl)piperidin-3-yl(methyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 2 h / 0 °C

2: 0.40 g / Et₃N / PdCl₂(PPh₃)2; CuI / acetonitrile / 16 h / 70 °C

With triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In dichloromethane; acetonitrile;
DOI:10.1021/jm061112p

Reference yield:

: 884602-81-7
(S)-tert-butyl 1-(2-nitro-4-(trifluoromethyl)phenyl)piperidin-3-ylcarbamate

: 884602-88-4
(S)-tert-butyl 1-(2-(5-(2-(2-aminopyrimidin-5-yl)ethynyl)-2-fluorobenzamido)-4-(trifluoromethyl)phenyl)piperidin-3-yl(methyl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: NaH / dimethylformamide / 0.33 h / 0 °C

1.2: dimethylformamide / 0.5 h / 0 - 20 °C

2.1: 89 percent / H₂ / Pd/C / methanol; H₂O / 8 h

3.1: Et₃N / CH₂Cl₂ / 2 h / 0 °C

4.1: 0.40 g / Et₃N / PdCl₂(PPh₃)2; CuI / acetonitrile / 16 h / 70 °C

With hydrogen; sodium hydride; triethylamine; bis-triphenylphosphine-palladium(II) chloride; palladium on activated charcoal; copper(l) iodide; In methanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm061112p