but-3-yn-1-yl 4-((3,4-dioxo-2-(((1R,2R)-2-(piperidin-1-yl)cyclohexyl)amino)cyclobut-1-en-1-yl)amino)-2-(trifluoromethyl)benzoate

Base Information

Chemical Name:but-3-yn-1-yl 4-((3,4-dioxo-2-(((1R,2R)-2-(piperidin-1-yl)cyclohexyl)amino)cyclobut-1-en-1-yl)amino)-2-(trifluoromethyl)benzoate
CAS No.:1433953-95-7
Molecular Formula:C₂₇H₃₀F₃N₃O₄
Molecular Weight:517.548
Hs Code.:

Synonyms:but-3-yn-1-yl 4-((3,4-dioxo-2-(((1R,2R)-2-(piperidin-1-yl)cyclohexyl)amino)cyclobut-1-en-1-yl)amino)-2-(trifluoromethyl)benzoate

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Chemical Property of but-3-yn-1-yl 4-((3,4-dioxo-2-(((1R,2R)-2-(piperidin-1-yl)cyclohexyl)amino)cyclobut-1-en-1-yl)amino)-2-(trifluoromethyl)benzoate

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Technology Process of but-3-yn-1-yl 4-((3,4-dioxo-2-(((1R,2R)-2-(piperidin-1-yl)cyclohexyl)amino)cyclobut-1-en-1-yl)amino)-2-(trifluoromethyl)benzoate

There total 2 articles about but-3-yn-1-yl 4-((3,4-dioxo-2-(((1R,2R)-2-(piperidin-1-yl)cyclohexyl)amino)cyclobut-1-en-1-yl)amino)-2-(trifluoromethyl)benzoate 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: 77.0%

: 885677-91-8,824938-80-9,824938-98-9
(1R,2R)-N¹-piperidinyl-1,2-diaminocyclohexane

: 1433953-94-6
but-3-yn-1-yl 4-((2-methoxy-3,4-dioxocyclobut-1-en-1-yl)amino)-2-(trifluoromethyl)benzoate

: 1433953-95-7
but-3-yn-1-yl 4-((3,4-dioxo-2-(((1R,2R)-2-(piperidin-1-yl)cyclohexyl)amino)cyclobut-1-en-1-yl)amino)-2-(trifluoromethyl)benzoate

Guidance literature:: In dichloromethane; at 20 ℃; for 48h;
DOI:10.1002/adsc.201200526

Reference yield:

: 1433953-93-5
but-3-yn-1-yl 4-amino-2-(trifluoromethyl)benzoate

: 1433953-95-7
but-3-yn-1-yl 4-((3,4-dioxo-2-(((1R,2R)-2-(piperidin-1-yl)cyclohexyl)amino)cyclobut-1-en-1-yl)amino)-2-(trifluoromethyl)benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: methanol / 48 h / 20 °C

2: dichloromethane / 48 h / 20 °C

In methanol; dichloromethane;
DOI:10.1002/adsc.201200526

Reference yield: 82.0%

: 1433953-95-7
but-3-yn-1-yl 4-((3,4-dioxo-2-(((1R,2R)-2-(piperidin-1-yl)cyclohexyl)amino)cyclobut-1-en-1-yl)amino)-2-(trifluoromethyl)benzoate

: 622-79-7
benzyl azide

: 2-(1-benzyl-1H-1,2,3-triazol-4-yl)ethyl 4-((2,3-dioxo-4-(((1R,2R)-2-(piperidin-1-yl)cyclohexyl)amino)cyclobutyl)amino)-2-(trifluoromethyl)benzoate

Guidance literature:: With tris(1-benzyl-1H-1,2,3-triazol-4-yl)methanol*CuCl; In tetrahydrofuran; at 80 ℃; for 3.33333h; Microwave irradiation;
DOI:10.1002/adsc.201200526