5-(6-(ethylamino)-2-(4-fluorophenyl)-3-(1H-imidazol-2-yl)benzofuran-5-yl)-2-methoxy-N-(1-(pyrimidin-2-yl)cyclopropyl)benzamide

Base Information

Chemical Name:5-(6-(ethylamino)-2-(4-fluorophenyl)-3-(1H-imidazol-2-yl)benzofuran-5-yl)-2-methoxy-N-(1-(pyrimidin-2-yl)cyclopropyl)benzamide
CAS No.:1449332-80-2
Molecular Formula:C₃₄H₂₉FN₆O₃
Molecular Weight:588.641
Hs Code.:

Synonyms:5-(6-(ethylamino)-2-(4-fluorophenyl)-3-(1H-imidazol-2-yl)benzofuran-5-yl)-2-methoxy-N-(1-(pyrimidin-2-yl)cyclopropyl)benzamide

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Chemical Property of 5-(6-(ethylamino)-2-(4-fluorophenyl)-3-(1H-imidazol-2-yl)benzofuran-5-yl)-2-methoxy-N-(1-(pyrimidin-2-yl)cyclopropyl)benzamide

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Technology Process of 5-(6-(ethylamino)-2-(4-fluorophenyl)-3-(1H-imidazol-2-yl)benzofuran-5-yl)-2-methoxy-N-(1-(pyrimidin-2-yl)cyclopropyl)benzamide

There total 1 articles about 5-(6-(ethylamino)-2-(4-fluorophenyl)-3-(1H-imidazol-2-yl)benzofuran-5-yl)-2-methoxy-N-(1-(pyrimidin-2-yl)cyclopropyl)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:

: 1449332-98-2
tert-butyl 2-(2-(4-fluorophenyl)-5-(4-methoxy-3-((1-(pyrimidin-2-yl)cyclopropyl)carbamoyl)phenyl)-6-nitrobenzofuran-3-yl)-1H-imidazole-1-carboxylate

: 75-07-0,9002-91-9
acetaldehyde

: 1449332-80-2
5-(6-(ethylamino)-2-(4-fluorophenyl)-3-(1H-imidazol-2-yl)benzofuran-5-yl)-2-methoxy-N-(1-(pyrimidin-2-yl)cyclopropyl)benzamide

: 1449333-02-1
tert-butyl 2-(6-(ethylamino)-2-(4-fluorophenyl)-5-(4-methoxy-3-((1-(pyrimidin-2-yl)cyclopropyl)carbamoyl)phenyl)benzofuran-3-yl)-1H-imidazole-1-carboxylate

Guidance literature:: tert-butyl 2-(2-(4-fluorophenyl)-5-(4-methoxy-3-((1-(pyrimidin-2-yl)cyclopropyl)carbamoyl)phenyl)-6-nitrobenzofuran-3-yl)-1H-imidazole-1-carboxylate; With indium; ammonium chloride; In ethanol; at 20 - 90 ℃; for 2.75h;

acetaldehyde; In methanol; at 0 - 20 ℃;

With sodium cyanoborohydride; In methanol; at 0 - 20 ℃; for 2h;

Reference yield:

: 1449332-80-2
5-(6-(ethylamino)-2-(4-fluorophenyl)-3-(1H-imidazol-2-yl)benzofuran-5-yl)-2-methoxy-N-(1-(pyrimidin-2-yl)cyclopropyl)benzamide

: 124-63-0
methanesulfonyl chloride

: 1449333-04-3
5-(6-N-(ethyl)methylsulfonamido-2-(4-fluorophenyl)-3-(1-(methylsulfonyl)-1H-imidazol-2-yl)benzofuran-5-yl)-2-methoxy-N-(1-(pyrimidin-2-yl)cyclopropyl)benzamide

Guidance literature:: With pyridine; dmap; at 20 ℃;

Reference yield:

: 1449332-80-2
5-(6-(ethylamino)-2-(4-fluorophenyl)-3-(1H-imidazol-2-yl)benzofuran-5-yl)-2-methoxy-N-(1-(pyrimidin-2-yl)cyclopropyl)benzamide

: 1449332-81-3
5-(6-(N-ethylmethylsulfonamido)-2-(4-fluorophenyl)-3-(1H-imidazol-2-yl)benzofuran-5-yl)-2-methoxy-N-(1-(pyrimidin-2-yl)cyclopropyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine; dmap / 20 °C

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 0 °C

With pyridine; dmap; tetrabutyl ammonium fluoride; In tetrahydrofuran;