ethyl 6-[2-(2-tert-butoxycarbonylamino-4-methoxyphenyl)-3-oxo-3-thiophen-3-ylpropyl]pyridine-2-carboxylate

Base Information

Chemical Name:ethyl 6-[2-(2-tert-butoxycarbonylamino-4-methoxyphenyl)-3-oxo-3-thiophen-3-ylpropyl]pyridine-2-carboxylate
CAS No.:1262880-53-4
Molecular Formula:C₂₇H₃₀N₂O₆S
Molecular Weight:510.611
Hs Code.:

Synonyms:ethyl 6-[2-(2-tert-butoxycarbonylamino-4-methoxyphenyl)-3-oxo-3-thiophen-3-ylpropyl]pyridine-2-carboxylate

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Chemical Property of ethyl 6-[2-(2-tert-butoxycarbonylamino-4-methoxyphenyl)-3-oxo-3-thiophen-3-ylpropyl]pyridine-2-carboxylate

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Technology Process of ethyl 6-[2-(2-tert-butoxycarbonylamino-4-methoxyphenyl)-3-oxo-3-thiophen-3-ylpropyl]pyridine-2-carboxylate

There total 6 articles about ethyl 6-[2-(2-tert-butoxycarbonylamino-4-methoxyphenyl)-3-oxo-3-thiophen-3-ylpropyl]pyridine-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:

: 1262879-55-9
tert-butyl [5-methoxy-2-(2-oxo-2-thiophen-3-ylethyl)phenyl]carbamate

: 49668-99-7
ethyl 6-chloromethylpyridine-2-carboxylate

: 1262880-53-4
ethyl 6-[2-(2-tert-butoxycarbonylamino-4-methoxyphenyl)-3-oxo-3-thiophen-3-ylpropyl]pyridine-2-carboxylate

Guidance literature:: tert-butyl [5-methoxy-2-(2-oxo-2-thiophen-3-ylethyl)phenyl]carbamate; With sodium hydride; In N,N-dimethyl-formamide; mineral oil; for 0.5h; Inert atmosphere; Cooling with ice;

ethyl 6-chloromethylpyridine-2-carboxylate; In N,N-dimethyl-formamide; mineral oil; at 20 ℃; for 6.33h; Inert atmosphere; Cooling with ice;

Reference yield:

: 138343-79-0
(5-methoxy-2-methyl-phenyl)-carbamic acid t-butyl ester

: 1262880-53-4
ethyl 6-[2-(2-tert-butoxycarbonylamino-4-methoxyphenyl)-3-oxo-3-thiophen-3-ylpropyl]pyridine-2-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: sec.-butyllithium / cyclohexane; hexane; tetrahydrofuran / 0.58 h / -43 °C / Inert atmosphere

1.2: 1.5 h / -45 - 20 °C

1.3: Cooling with ice

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / Inert atmosphere; Cooling with ice

2.2: 6.33 h / 20 °C / Inert atmosphere; Cooling with ice

With sec.-butyllithium; sodium hydride; In tetrahydrofuran; hexane; cyclohexane; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1262880-53-4
ethyl 6-[2-(2-tert-butoxycarbonylamino-4-methoxyphenyl)-3-oxo-3-thiophen-3-ylpropyl]pyridine-2-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrahydrofuran / Reflux

2.1: sec.-butyllithium / cyclohexane; hexane; tetrahydrofuran / 0.58 h / -43 °C / Inert atmosphere

2.2: 1.5 h / -45 - 20 °C

2.3: Cooling with ice

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / Inert atmosphere; Cooling with ice

3.2: 6.33 h / 20 °C / Inert atmosphere; Cooling with ice

With sec.-butyllithium; sodium hydride; In tetrahydrofuran; hexane; cyclohexane; N,N-dimethyl-formamide; mineral oil;