methyl 5-(3,3-dimethylbut-1-ynyl)-3-((1r,4R)-4-methyl-N-((1s,4S)-4-(pyridin-3-yloxy)cyclohexyl)cyclohexanecarboxamido)thiophene-2-carboxylate

Base Information

Chemical Name:methyl 5-(3,3-dimethylbut-1-ynyl)-3-((1r,4R)-4-methyl-N-((1s,4S)-4-(pyridin-3-yloxy)cyclohexyl)cyclohexanecarboxamido)thiophene-2-carboxylate
CAS No.:1485470-01-6
Molecular Formula:C₃₁H₄₀N₂O₄S
Molecular Weight:536.736
Hs Code.:

methyl 5-(3,3-dimethylbut-1-ynyl)-3-((1r,4R)-4-methyl-N-((1s,4S)-4-(pyridin-3-yloxy)cyclohexyl)cyclohexanecarboxamido)thiophene-2-carboxylate

Synonyms:

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Chemical Property of methyl 5-(3,3-dimethylbut-1-ynyl)-3-((1r,4R)-4-methyl-N-((1s,4S)-4-(pyridin-3-yloxy)cyclohexyl)cyclohexanecarboxamido)thiophene-2-carboxylate

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Technology Process of methyl 5-(3,3-dimethylbut-1-ynyl)-3-((1r,4R)-4-methyl-N-((1s,4S)-4-(pyridin-3-yloxy)cyclohexyl)cyclohexanecarboxamido)thiophene-2-carboxylate

There total 10 articles about methyl 5-(3,3-dimethylbut-1-ynyl)-3-((1r,4R)-4-methyl-N-((1s,4S)-4-(pyridin-3-yloxy)cyclohexyl)cyclohexanecarboxamido)thiophene-2-carboxylate 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: 37.0%

: 109-00-2
3-HYDROXYPYRIDINE

: 1026785-63-6
methyl 5-(3,3-dimethylbut-1-ynyl)-3-[(trans-4-hydroxycyclohexyl)-(trans-4-methylcyclohexanecarbonyl)amino]thiophene-2-carboxylate

: 1485470-01-6
methyl 5-(3,3-dimethylbut-1-ynyl)-3-((1r,4R)-4-methyl-N-((1s,4S)-4-(pyridin-3-yloxy)cyclohexyl)cyclohexanecarboxamido)thiophene-2-carboxylate

Guidance literature:: With di-isopropyl azodicarboxylate; triethylamine; triphenylphosphine; In tetrahydrofuran; at 20 ℃; for 12h; Inert atmosphere;
DOI:10.1021/jm401420j

Reference yield:

: 934-67-8,4331-54-8,13064-83-0
trans-4-methylcyclohexanecarboxylic acid

: 1485470-01-6
methyl 5-(3,3-dimethylbut-1-ynyl)-3-((1r,4R)-4-methyl-N-((1s,4S)-4-(pyridin-3-yloxy)cyclohexyl)cyclohexanecarboxamido)thiophene-2-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1.1: dichloromethane; N,N-dimethyl-formamide / 3 h / 0 - 20 °C

2.1: pyridine / toluene / 16 h / Reflux

3.1: n-butyllithium; diisopropylamine / tetrahydrofuran; hexane / 2 h / -75 - -60 °C

3.2: 3 h / -78 °C

4.1: copper(l) iodide; triethylamine; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex / N,N-dimethyl-formamide / 12 h / 60 °C / Inert atmosphere

5.1: hydrogenchloride / tetrahydrofuran; water / 12 h / 40 °C

6.1: sodium tetrahydroborate / tetrahydrofuran / 2 h / -25 °C

7.1: triphenylphosphine; di-isopropyl azodicarboxylate; triethylamine / tetrahydrofuran / 12 h / 20 °C / Inert atmosphere

With pyridine; hydrogenchloride; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; sodium tetrahydroborate; copper(l) iodide; n-butyllithium; di-isopropyl azodicarboxylate; triethylamine; diisopropylamine; triphenylphosphine; In tetrahydrofuran; hexane; dichloromethane; water; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jm401420j

Reference yield:

: 55930-23-9
trans-4-methylcyclohexanecarbonyl chloride

: 1485470-01-6
methyl 5-(3,3-dimethylbut-1-ynyl)-3-((1r,4R)-4-methyl-N-((1s,4S)-4-(pyridin-3-yloxy)cyclohexyl)cyclohexanecarboxamido)thiophene-2-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1.1: pyridine / toluene / 16 h / Reflux

2.1: n-butyllithium; diisopropylamine / tetrahydrofuran; hexane / 2 h / -75 - -60 °C

2.2: 3 h / -78 °C

3.1: copper(l) iodide; triethylamine; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex / N,N-dimethyl-formamide / 12 h / 60 °C / Inert atmosphere

4.1: hydrogenchloride / tetrahydrofuran; water / 12 h / 40 °C

5.1: sodium tetrahydroborate / tetrahydrofuran / 2 h / -25 °C

6.1: triphenylphosphine; di-isopropyl azodicarboxylate; triethylamine / tetrahydrofuran / 12 h / 20 °C / Inert atmosphere

With pyridine; hydrogenchloride; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; sodium tetrahydroborate; copper(l) iodide; n-butyllithium; di-isopropyl azodicarboxylate; triethylamine; diisopropylamine; triphenylphosphine; In tetrahydrofuran; hexane; water; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jm401420j