(5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl)(3-(4-(pyrrolidin-1-ylmethyl)phenoxy)azetidin-1-yl)methanone

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Chemical Name:(5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl)(3-(4-(pyrrolidin-1-ylmethyl)phenoxy)azetidin-1-yl)methanone
CAS No.:1354791-20-0
Molecular Formula:C₂₃H₂₃ClN₄O₃
Molecular Weight:438.914
Hs Code.:

Synonyms:(5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl)(3-(4-(pyrrolidin-1-ylmethyl)phenoxy)azetidin-1-yl)methanone

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Chemical Property of (5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl)(3-(4-(pyrrolidin-1-ylmethyl)phenoxy)azetidin-1-yl)methanone

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Technology Process of (5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl)(3-(4-(pyrrolidin-1-ylmethyl)phenoxy)azetidin-1-yl)methanone

There total 3 articles about (5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl)(3-(4-(pyrrolidin-1-ylmethyl)phenoxy)azetidin-1-yl)methanone 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: 24.0%

: 68496-88-8
ethyl 5-(4-chlorophenyl)-1,3,4-oxadiazole-2-carboxylate

: 1354792-30-5
1-(4-(azetidin-3-yloxy)benzyl)pyrrolidine

: 1354791-20-0
(5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl)(3-(4-(pyrrolidin-1-ylmethyl)phenoxy)azetidin-1-yl)methanone

Guidance literature:: at 120 ℃; for 4h;

Reference yield:

: 72219-19-3
4-((pyrrolidin-1-yl)methyl)phenol

: 1354791-20-0
(5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl)(3-(4-(pyrrolidin-1-ylmethyl)phenoxy)azetidin-1-yl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / Inert atmosphere; Cooling with ice

1.2: 80 °C / Inert atmosphere

2.1: trifluoroacetic acid / dichloromethane / 17 h / 20 °C

2.2: pH 10

3.1: 4 h / 120 °C

With sodium hydride; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 1354792-29-2
tert-butyl 3-(4-(pyrrolidin-1-ylmethyl)phenoxy)azetidine-1-carboxylate

: 1354791-20-0
(5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl)(3-(4-(pyrrolidin-1-ylmethyl)phenoxy)azetidin-1-yl)methanone

Guidance literature:: Multi-step reaction with 2 steps

1.1: trifluoroacetic acid / dichloromethane / 17 h / 20 °C

1.2: pH 10

2.1: 4 h / 120 °C

With trifluoroacetic acid; In dichloromethane;