1,10-bis{3-[2-(2-aminophenyl)-4-hydroxycarbonylbenzimidazol-1-ylmethyl]phenoxy}decane

Base Information

Chemical Name:1,10-bis{3-[2-(2-aminophenyl)-4-hydroxycarbonylbenzimidazol-1-ylmethyl]phenoxy}decane
CAS No.:560086-46-6
Molecular Formula:C₅₂H₅₂N₆O₆
Molecular Weight:857.021
Hs Code.:

Synonyms:1,10-bis{3-[2-(2-aminophenyl)-4-hydroxycarbonylbenzimidazol-1-ylmethyl]phenoxy}decane

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Chemical Property of 1,10-bis{3-[2-(2-aminophenyl)-4-hydroxycarbonylbenzimidazol-1-ylmethyl]phenoxy}decane

Chemical Property:

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Technology Process of 1,10-bis{3-[2-(2-aminophenyl)-4-hydroxycarbonylbenzimidazol-1-ylmethyl]phenoxy}decane

There total 9 articles about 1,10-bis{3-[2-(2-aminophenyl)-4-hydroxycarbonylbenzimidazol-1-ylmethyl]phenoxy}decane 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:

: 560086-42-2
1,10-bis{3-[2-(2-aminophenyl)-4-ethoxycarbonylbenzimidazol-1-ylmethyl]phenoxy}decane

: 560086-46-6
1,10-bis{3-[2-(2-aminophenyl)-4-hydroxycarbonylbenzimidazol-1-ylmethyl]phenoxy}decane

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; at 20 ℃; for 16h;
DOI:10.1021/ja030196d

Reference yield:

: 552-16-9,104810-18-6
ortho-nitrobenzoic acid

: 560086-46-6
1,10-bis{3-[2-(2-aminophenyl)-4-hydroxycarbonylbenzimidazol-1-ylmethyl]phenoxy}decane

Guidance literature:: Multi-step reaction with 5 steps

1.1: oxalyl chloride; DMF / CH₂Cl₂ / 12 h / 20 °C

2.1: Et₃N / CH₂Cl₂ / 4 h / 0 - 20 °C

2.2: 93 percent / AcONa / acetic acid / 15 h / Heating

3.1: NaH / tetrahydrofuran / 0 - 20 °C

3.2: 93 percent / tetrahydrofuran / 20 h / 20 °C

4.1: 93 percent / SnCl₂; EtOH / 0.75 h / Heating

5.1: aq. LiOH / tetrahydrofuran / 16 h / 20 °C

With lithium hydroxide; oxalyl dichloride; ethanol; sodium hydride; triethylamine; N,N-dimethyl-formamide; tin(ll) chloride; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja030196d

Reference yield:

: 620-24-6
3-Hydroxybenzyl alcohol

: 560086-46-6
1,10-bis{3-[2-(2-aminophenyl)-4-hydroxycarbonylbenzimidazol-1-ylmethyl]phenoxy}decane

Guidance literature:: Multi-step reaction with 5 steps

1.1: 70 percent / aq. NaOH / ethanol / 18 h / Heating

2.1: 79 percent / PBr₃ / CH₂Cl₂ / 18 h / 20 °C

3.1: NaH / tetrahydrofuran / 0 - 20 °C

3.2: 93 percent / tetrahydrofuran / 20 h / 20 °C

4.1: 93 percent / SnCl₂; EtOH / 0.75 h / Heating

5.1: aq. LiOH / tetrahydrofuran / 16 h / 20 °C

With lithium hydroxide; sodium hydroxide; ethanol; phosphorus tribromide; sodium hydride; tin(ll) chloride; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1021/ja030196d