1-<3-(1,3,4-oxadiazol-2-yl)phenoxy>-3-<4-(2-methoxyphenyl)-1-piperazinyl>-2-propanol

Base Information

Chemical Name:1-<3-(1,3,4-oxadiazol-2-yl)phenoxy>-3-<4-(2-methoxyphenyl)-1-piperazinyl>-2-propanol
CAS No.:118778-80-6
Molecular Formula:C₂₂H₂₆N₄O₄
Molecular Weight:410.473
Hs Code.:

Synonyms:1-<3-(1,3,4-oxadiazol-2-yl)phenoxy>-3-<4-(2-methoxyphenyl)-1-piperazinyl>-2-propanol

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Chemical Property of 1-<3-(1,3,4-oxadiazol-2-yl)phenoxy>-3-<4-(2-methoxyphenyl)-1-piperazinyl>-2-propanol

Chemical Property:

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Technology Process of 1-<3-(1,3,4-oxadiazol-2-yl)phenoxy>-3-<4-(2-methoxyphenyl)-1-piperazinyl>-2-propanol

There total 5 articles about 1-<3-(1,3,4-oxadiazol-2-yl)phenoxy>-3-<4-(2-methoxyphenyl)-1-piperazinyl>-2-propanol 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:

: 777806-20-9
1-[2-(1,3,4-oxadiazol-2-yl)-phenoxy]-3-[4-(2-methoxyphenyl)-piperazin-1-yl]-propan-2-ol

: 118778-80-6
1-<3-(1,3,4-oxadiazol-2-yl)phenoxy>-3-<4-(2-methoxyphenyl)-1-piperazinyl>-2-propanol

Guidance literature:: In ethanol;

Reference yield:

: 5378-29-0
2-(3-hydroxyphenyl)-1,3,4-oxadiazole

: 118778-80-6
1-<3-(1,3,4-oxadiazol-2-yl)phenoxy>-3-<4-(2-methoxyphenyl)-1-piperazinyl>-2-propanol

Guidance literature:: Multi-step reaction with 2 steps

1: 53 percent / NaH / dimethylsulfoxide / 7 h / Ambient temperature

2: ethanol / 17 h / Heating

With sodium hydride; In ethanol; dimethyl sulfoxide;
DOI:10.1016/S0040-4020(01)85962-7

Reference yield:

: 19438-10-9
methyl 3-hydroxybenzoate

: 118778-80-6
1-<3-(1,3,4-oxadiazol-2-yl)phenoxy>-3-<4-(2-methoxyphenyl)-1-piperazinyl>-2-propanol

Guidance literature:: Multi-step reaction with 4 steps

1: N₂H_4.H₂O / methanol

2: 86 percent / 22 h / Heating

3: 53 percent / NaH / dimethylsulfoxide / 7 h / Ambient temperature

4: ethanol / 17 h / Heating

With sodium hydride; hydrazine hydrate; In methanol; ethanol; dimethyl sulfoxide;
DOI:10.1016/S0040-4020(01)85962-7