N-(1-(4-(1H-tetrazol-5-yl)phenyl)cyclopropyl)-5-chloro-2-(3-(3-fluorophenoxy)-azetidin-1-yl)nicotinamide

Base Information

Chemical Name:N-(1-(4-(1H-tetrazol-5-yl)phenyl)cyclopropyl)-5-chloro-2-(3-(3-fluorophenoxy)-azetidin-1-yl)nicotinamide
CAS No.:1380752-14-6
Molecular Formula:C₂₅H₂₁ClFN₇O₂
Molecular Weight:505.939
Hs Code.:

Synonyms:N-(1-(4-(1H-tetrazol-5-yl)phenyl)cyclopropyl)-5-chloro-2-(3-(3-fluorophenoxy)-azetidin-1-yl)nicotinamide

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Chemical Property of N-(1-(4-(1H-tetrazol-5-yl)phenyl)cyclopropyl)-5-chloro-2-(3-(3-fluorophenoxy)-azetidin-1-yl)nicotinamide

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Technology Process of N-(1-(4-(1H-tetrazol-5-yl)phenyl)cyclopropyl)-5-chloro-2-(3-(3-fluorophenoxy)-azetidin-1-yl)nicotinamide

There total 4 articles about N-(1-(4-(1H-tetrazol-5-yl)phenyl)cyclopropyl)-5-chloro-2-(3-(3-fluorophenoxy)-azetidin-1-yl)nicotinamide 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:

: 1380753-33-2
methyl 5-chloro-2-(3-(3-fluorophenoxy)azetidin-1-yl)nicotinate

: 1380752-36-2
1-(4-(1H-tetrazol-5-yl)phenyl)cyclopropanamine hydrochloride

: 1380752-14-6
N-(1-(4-(1H-tetrazol-5-yl)phenyl)cyclopropyl)-5-chloro-2-(3-(3-fluorophenoxy)-azetidin-1-yl)nicotinamide

Guidance literature:: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 1h;

Reference yield:

: 67754-03-4
methyl 2,5-dichloronicotinate

: 1380752-14-6
N-(1-(4-(1H-tetrazol-5-yl)phenyl)cyclopropyl)-5-chloro-2-(3-(3-fluorophenoxy)-azetidin-1-yl)nicotinamide

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / tetrahydrofuran; methanol / 62 - 80 °C

2: triethylamine / N,N-dimethyl-formamide / 6.5 h / 0 °C

3: potassium carbonate / acetonitrile / 0.25 h / 150 - 180 °C / Microwave irradiation

4: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 1 h / 20 °C

With potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1380753-11-6
methyl 5-chloro-2-(3-hydroxyazetidin-1-yl)nicotinate

: 1380752-14-6
N-(1-(4-(1H-tetrazol-5-yl)phenyl)cyclopropyl)-5-chloro-2-(3-(3-fluorophenoxy)-azetidin-1-yl)nicotinamide

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / N,N-dimethyl-formamide / 6.5 h / 0 °C

2: potassium carbonate / acetonitrile / 0.25 h / 150 - 180 °C / Microwave irradiation

3: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 1 h / 20 °C

With potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide; acetonitrile;