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1-{6-[5-(4-chloro-phenyl)-[1,2,4]oxadiazol-3-ylmethoxy]-indanyl}-4-acetyl-piperazine

Base Information
  • Chemical Name:1-{6-[5-(4-chloro-phenyl)-[1,2,4]oxadiazol-3-ylmethoxy]-indanyl}-4-acetyl-piperazine
  • CAS No.:935248-14-9
  • Molecular Formula:C24H25ClN4O3
  • Molecular Weight:452.941
  • Hs Code.:
1-{6-[5-(4-chloro-phenyl)-[1,2,4]oxadiazol-3-ylmethoxy]-indanyl}-4-acetyl-piperazine

Synonyms:1-{6-[5-(4-chloro-phenyl)-[1,2,4]oxadiazol-3-ylmethoxy]-indanyl}-4-acetyl-piperazine

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Chemical Property of 1-{6-[5-(4-chloro-phenyl)-[1,2,4]oxadiazol-3-ylmethoxy]-indanyl}-4-acetyl-piperazine
Chemical Property:
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Technology Process of 1-{6-[5-(4-chloro-phenyl)-[1,2,4]oxadiazol-3-ylmethoxy]-indanyl}-4-acetyl-piperazine

There total 5 articles about 1-{6-[5-(4-chloro-phenyl)-[1,2,4]oxadiazol-3-ylmethoxy]-indanyl}-4-acetyl-piperazine 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:
Guidance literature:
Multi-step reaction with 5 steps
1: sodium borohydride / methanol / 1 h / 20 °C
2: thionyl chloride / toluene / 1.5 h / 20 - 60 °C
3: 4.6 g / potassium carbonate / tetrabutylammonium iodide / acetonitrile / 16 h / 70 - 75 °C
4: 62 percent / BBr3 / tetrabutylammonium iodide / CH2Cl2 / 14 h / 20 °C
5: 65 percent / cesium carbonate / tetrabutylammonium iodide / acetonitrile / 40 h / 60 - 65 °C
With sodium tetrahydroborate; thionyl chloride; boron tribromide; potassium carbonate; caesium carbonate; tetra-(n-butyl)ammonium iodide; In methanol; dichloromethane; toluene; acetonitrile;
DOI:10.1016/j.bmcl.2006.12.109
Guidance literature:
Multi-step reaction with 4 steps
1: thionyl chloride / toluene / 1.5 h / 20 - 60 °C
2: 4.6 g / potassium carbonate / tetrabutylammonium iodide / acetonitrile / 16 h / 70 - 75 °C
3: 62 percent / BBr3 / tetrabutylammonium iodide / CH2Cl2 / 14 h / 20 °C
4: 65 percent / cesium carbonate / tetrabutylammonium iodide / acetonitrile / 40 h / 60 - 65 °C
With thionyl chloride; boron tribromide; potassium carbonate; caesium carbonate; tetra-(n-butyl)ammonium iodide; In dichloromethane; toluene; acetonitrile;
DOI:10.1016/j.bmcl.2006.12.109
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