(2-(3-(tert-butyldimethylsilyloxy)propyl)-4-hydroxy-4-(2-methoxyphenyl)piperidin-1-yl)((2R,3S)-2-propyl-1-(3-(trifluoromethyl)picolinoyl)-3-(5-(trifluoromethyl)thiophen-3-yloxy)piperidin-3-yl)methanone

Base Information

Chemical Name:(2-(3-(tert-butyldimethylsilyloxy)propyl)-4-hydroxy-4-(2-methoxyphenyl)piperidin-1-yl)((2R,3S)-2-propyl-1-(3-(trifluoromethyl)picolinoyl)-3-(5-(trifluoromethyl)thiophen-3-yloxy)piperidin-3-yl)methanone
CAS No.:1292307-34-6
Molecular Formula:C₄₂H₅₅F₆N₃O₆SSi
Molecular Weight:872.057
Hs Code.:

(2-(3-(tert-butyldimethylsilyloxy)propyl)-4-hydroxy-4-(2-methoxyphenyl)piperidin-1-yl)((2R,3S)-2-propyl-1-(3-(trifluoromethyl)picolinoyl)-3-(5-(trifluoromethyl)thiophen-3-yloxy)piperidin-3-yl)methanone

Synonyms:(2-(3-(tert-butyldimethylsilyloxy)propyl)-4-hydroxy-4-(2-methoxyphenyl)piperidin-1-yl)((2R,3S)-2-propyl-1-(3-(trifluoromethyl)picolinoyl)-3-(5-(trifluoromethyl)thiophen-3-yloxy)piperidin-3-yl)methanone

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Chemical Property of (2-(3-(tert-butyldimethylsilyloxy)propyl)-4-hydroxy-4-(2-methoxyphenyl)piperidin-1-yl)((2R,3S)-2-propyl-1-(3-(trifluoromethyl)picolinoyl)-3-(5-(trifluoromethyl)thiophen-3-yloxy)piperidin-3-yl)methanone

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Technology Process of (2-(3-(tert-butyldimethylsilyloxy)propyl)-4-hydroxy-4-(2-methoxyphenyl)piperidin-1-yl)((2R,3S)-2-propyl-1-(3-(trifluoromethyl)picolinoyl)-3-(5-(trifluoromethyl)thiophen-3-yloxy)piperidin-3-yl)methanone

There total 8 articles about (2-(3-(tert-butyldimethylsilyloxy)propyl)-4-hydroxy-4-(2-methoxyphenyl)piperidin-1-yl)((2R,3S)-2-propyl-1-(3-(trifluoromethyl)picolinoyl)-3-(5-(trifluoromethyl)thiophen-3-yloxy)piperidin-3-yl)methanone 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:

: 1292307-33-5
2-(3-(tert-butyldimethylsilyloxy)propyl)-4-(2-methoxyphenyl)piperidin-4-ol

: 1292306-76-3
(2R,3S)-2-propyl-1-(3-(trifluoromethyl)picolinoyl)-3-(5-(trifluoromethyl)thiophen-3-yloxy)piperidine-3-carbonyl chloride

: 1292307-34-6
(2-(3-(tert-butyldimethylsilyloxy)propyl)-4-hydroxy-4-(2-methoxyphenyl)piperidin-1-yl)((2R,3S)-2-propyl-1-(3-(trifluoromethyl)picolinoyl)-3-(5-(trifluoromethyl)thiophen-3-yloxy)piperidin-3-yl)methanone

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 16h;

Reference yield:

: 620-08-6,1232006-56-2
4-methoxypyridine

: 1292307-34-6
(2-(3-(tert-butyldimethylsilyloxy)propyl)-4-hydroxy-4-(2-methoxyphenyl)piperidin-1-yl)((2R,3S)-2-propyl-1-(3-(trifluoromethyl)picolinoyl)-3-(5-(trifluoromethyl)thiophen-3-yloxy)piperidin-3-yl)methanone

Guidance literature:: Multi-step reaction with 7 steps

1.1: diethyl ether; tetrahydrofuran / 0.5 h / -23 °C

2.1: zinc; acetic acid / 16 h / 50 °C

3.1: diethyl ether; tetrahydrofuran / 2 h / -78 °C

4.1: 9-bora-bicyclo[3.3.1]nonane / tetrahydrofuran / 16 h / 20 °C

4.2: 0.5 h

5.1: triethylamine / dmap / dichloromethane / 16 h / 0 - 20 °C

6.1: hydrogen / palladium-on-charcoal / ethyl acetate / 2 h

7.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 16 h / 20 °C

With hydrogen; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; 9-bora-bicyclo[3.3.1]nonane; zinc; dmap; palladium-on-charcoal; In tetrahydrofuran; diethyl ether; dichloromethane; ethyl acetate;

Reference yield:

: 1292307-29-9
benzyl 2-allyl-4-oxopiperidine-1-carboxylate

: 1292307-34-6
(2-(3-(tert-butyldimethylsilyloxy)propyl)-4-hydroxy-4-(2-methoxyphenyl)piperidin-1-yl)((2R,3S)-2-propyl-1-(3-(trifluoromethyl)picolinoyl)-3-(5-(trifluoromethyl)thiophen-3-yloxy)piperidin-3-yl)methanone

Guidance literature:: Multi-step reaction with 5 steps

1.1: diethyl ether; tetrahydrofuran / 2 h / -78 °C

2.1: 9-bora-bicyclo[3.3.1]nonane / tetrahydrofuran / 16 h / 20 °C

2.2: 0.5 h

3.1: triethylamine / dmap / dichloromethane / 16 h / 0 - 20 °C

4.1: hydrogen / palladium-on-charcoal / ethyl acetate / 2 h

5.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 16 h / 20 °C

With hydrogen; triethylamine; N-ethyl-N,N-diisopropylamine; 9-bora-bicyclo[3.3.1]nonane; dmap; palladium-on-charcoal; In tetrahydrofuran; diethyl ether; dichloromethane; ethyl acetate;