4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)-N-({1-[4,5,5,5-tetrafluoro-4-(trifluoromethyl)pentyl]piperidin-4-yl}methyl)benzamide

Base Information

Chemical Name:4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)-N-({1-[4,5,5,5-tetrafluoro-4-(trifluoromethyl)pentyl]piperidin-4-yl}methyl)benzamide
CAS No.:1093396-21-4
Molecular Formula:C₃₀H₃₁F₇N₄O₂
Molecular Weight:612.591
Hs Code.:

Synonyms:4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)-N-({1-[4,5,5,5-tetrafluoro-4-(trifluoromethyl)pentyl]piperidin-4-yl}methyl)benzamide

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Chemical Property of 4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)-N-({1-[4,5,5,5-tetrafluoro-4-(trifluoromethyl)pentyl]piperidin-4-yl}methyl)benzamide

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Technology Process of 4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)-N-({1-[4,5,5,5-tetrafluoro-4-(trifluoromethyl)pentyl]piperidin-4-yl}methyl)benzamide

There total 9 articles about 4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)-N-({1-[4,5,5,5-tetrafluoro-4-(trifluoromethyl)pentyl]piperidin-4-yl}methyl)benzamide 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:

: C₆H₅F₇O

: 1093396-14-5
4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)-N-(piperidin-4-ylmethyl)benzamide

: 1093396-21-4
4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)-N-({1-[4,5,5,5-tetrafluoro-4-(trifluoromethyl)pentyl]piperidin-4-yl}methyl)benzamide

Guidance literature:: With sodium cyanoborohydride; In methanol; at 20 ℃;

Reference yield:

: 29819-73-6
4,5,5,5-tetrafluoro-4-trifluoromethyl-1-pentanol

: 1093396-21-4
4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)-N-({1-[4,5,5,5-tetrafluoro-4-(trifluoromethyl)pentyl]piperidin-4-yl}methyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 4-methylmorpholine N-oxide / tetrapropylammonium perruthennate / dichloromethane / 1 h / 20 °C / Molecular sieve

2: sodium cyanoborohydride / methanol / 20 °C

With sodium cyanoborohydride; 4-methylmorpholine N-oxide; tetrapropylammonium perruthennate; In methanol; dichloromethane;

Reference yield:

: 1828-58-6
3-bromo-4-hydroxy-5-nitrobenzonitrile

: 1093396-21-4
4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)-N-({1-[4,5,5,5-tetrafluoro-4-(trifluoromethyl)pentyl]piperidin-4-yl}methyl)benzamide

Guidance literature:: Multi-step reaction with 8 steps

1.1: pyrographite / iron(III) chloride / methanol / 0.25 h / 65 °C

1.2: 2 h / Reflux

2.1: 1,4-dioxane / Reflux

2.2: Reflux

3.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / ethanol; water; toluene / 91 °C / Inert atmosphere

4.1: hydrogen / palladium 10% on activated carbon / tetrahydrofuran / 3 h / 60 °C / 517.16 Torr

5.1: lithium hydroxide monohydrate / tetrahydrofuran; methanol; water / 1 h / 50 °C

5.2: 0.08 h

6.1: oxalyl dichloride / dichloromethane; N,N-dimethyl-formamide / 1 h / 25 °C

6.2: 25 °C

7.1: hydrogen / palladium 10% on activated carbon / tetrahydrofuran; methanol / 3 h / 50 °C

8.1: sodium cyanoborohydride / methanol / 20 °C

With oxalyl dichloride; lithium hydroxide monohydrate; hydrogen; sodium cyanoborohydride; sodium carbonate; pyrographite; iron(III) chloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene;