(5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl)(3-(4-(pyrrolidin-1-ylmethyl)phenylthio)azetidin-1-yl)methanone

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Chemical Name:(5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl)(3-(4-(pyrrolidin-1-ylmethyl)phenylthio)azetidin-1-yl)methanone
CAS No.:1354791-79-9
Molecular Formula:C₂₄H₂₆N₄O₃S
Molecular Weight:450.561
Hs Code.:

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

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

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

There total 6 articles about (5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl)(3-(4-(pyrrolidin-1-ylmethyl)phenylthio)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%

: 1354792-73-6
1-(4-(Azetidin-3-ylthio)benzyl)pyrrolidine

: 99367-44-9
ethyl 5-(4-methoxyphenyl)-1,3,4-oxadiazole-2-carboxylate

: 1354791-79-9
(5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl)(3-(4-(pyrrolidin-1-ylmethyl)phenylthio)azetidin-1-yl)methanone

Guidance literature:: at 120 ℃; for 2h;

Reference yield:

: 6302-65-4
methyl 4-mercaptobenzoate

: 1354791-79-9
(5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl)(3-(4-(pyrrolidin-1-ylmethyl)phenylthio)azetidin-1-yl)methanone

Guidance literature:: Multi-step reaction with 6 steps

1.1: caesium carbonate / N,N-dimethyl-formamide / 3 h / 90 °C

2.1: water; lithium hydroxide / tetrahydrofuran / 15 h / 20 °C

2.2: pH 3 / Cooling with ice

3.1: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / dichloromethane / 1.83 h / 0 - 20 °C

4.1: hydrogenchloride / 1,4-dioxane / 20 °C

4.2: pH > 11

5.1: lithium aluminium tetrahydride / tetrahydrofuran / 5 h / 50 °C / Inert atmosphere

5.2: 1 h / Inert atmosphere; Cooling

6.1: 2 h / 120 °C

With hydrogenchloride; lithium aluminium tetrahydride; water; caesium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1354792-69-0
tert-Butyl 3-(4-(methoxycarbonyl)phenylthio)azetidine-1-carboxylate

: 1354791-79-9
(5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl)(3-(4-(pyrrolidin-1-ylmethyl)phenylthio)azetidin-1-yl)methanone

Guidance literature:: Multi-step reaction with 5 steps

1.1: water; lithium hydroxide / tetrahydrofuran / 15 h / 20 °C

1.2: pH 3 / Cooling with ice

2.1: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / dichloromethane / 1.83 h / 0 - 20 °C

3.1: hydrogenchloride / 1,4-dioxane / 20 °C

3.2: pH > 11

4.1: lithium aluminium tetrahydride / tetrahydrofuran / 5 h / 50 °C / Inert atmosphere

4.2: 1 h / Inert atmosphere; Cooling

5.1: 2 h / 120 °C

With hydrogenchloride; lithium aluminium tetrahydride; water; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; dichloromethane;