4'-((9-nitro-5,6-dihydro-2H-imidazo[2,1-b][1,3,6]oxadiazocin-4(3H)-yl)methyl)-[1,1'-biphenyl]-4-carboxylic acid

Base Information

Chemical Name:4'-((9-nitro-5,6-dihydro-2H-imidazo[2,1-b][1,3,6]oxadiazocin-4(3H)-yl)methyl)-[1,1'-biphenyl]-4-carboxylic acid
CAS No.:1437113-86-4
Molecular Formula:C₂₁H₂₀N₄O₅
Molecular Weight:408.414
Hs Code.:

Synonyms:4'-((9-nitro-5,6-dihydro-2H-imidazo[2,1-b][1,3,6]oxadiazocin-4(3H)-yl)methyl)-[1,1'-biphenyl]-4-carboxylic acid

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Chemical Property of 4'-((9-nitro-5,6-dihydro-2H-imidazo[2,1-b][1,3,6]oxadiazocin-4(3H)-yl)methyl)-[1,1'-biphenyl]-4-carboxylic acid

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Technology Process of 4'-((9-nitro-5,6-dihydro-2H-imidazo[2,1-b][1,3,6]oxadiazocin-4(3H)-yl)methyl)-[1,1'-biphenyl]-4-carboxylic acid

There total 4 articles about 4'-((9-nitro-5,6-dihydro-2H-imidazo[2,1-b][1,3,6]oxadiazocin-4(3H)-yl)methyl)-[1,1'-biphenyl]-4-carboxylic acid 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:

: 1437112-26-9
ethyl 4'-((9-nitro-5,6-dihydro-2H-imidazo[2,1-b][1,3,6]oxadiazocin-4(3H)-yl)methyl)-[1,1'-biphenyl]-4-carboxylate

: 1437113-86-4
4'-((9-nitro-5,6-dihydro-2H-imidazo[2,1-b][1,3,6]oxadiazocin-4(3H)-yl)methyl)-[1,1'-biphenyl]-4-carboxylic acid

Guidance literature:: With lithium hydroxide monohydrate; In methanol; at 20 ℃; for 16h;

Reference yield:

: 1437126-10-7
N-(2-((tert-butyldimethylsilyl)oxy)ethyl)-N-(2-(2,4-dinitro-1H-imidazol-1-yl)ethyl)prop-2-en-1-amine

: 1437113-86-4
4'-((9-nitro-5,6-dihydro-2H-imidazo[2,1-b][1,3,6]oxadiazocin-4(3H)-yl)methyl)-[1,1'-biphenyl]-4-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 48 h / 20 °C

2.1: carbonochloridic acid 1-chloro-ethyl ester / 1,2-dichloro-ethane / 0 - 90 °C / Cooling with ice; Reflux

3.1: potassium carbonate / acetonitrile; water / 0.17 h

3.2: 20 °C

4.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium carbonate / ethanol; water / 60 °C / Inert atmosphere

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; carbonochloridic acid 1-chloro-ethyl ester; tetrabutyl ammonium fluoride; sodium carbonate; potassium carbonate; In tetrahydrofuran; ethanol; water; 1,2-dichloro-ethane; acetonitrile;

Reference yield:

: 1437109-98-2
4-allyl-9-nitro-3,4,5,6-tetrahydro-2H-imidazo[2,1-b][1,3,6]oxadiazocine

: 1437113-86-4
4'-((9-nitro-5,6-dihydro-2H-imidazo[2,1-b][1,3,6]oxadiazocin-4(3H)-yl)methyl)-[1,1'-biphenyl]-4-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: carbonochloridic acid 1-chloro-ethyl ester / 1,2-dichloro-ethane / 0 - 90 °C / Cooling with ice; Reflux

2.1: potassium carbonate / acetonitrile; water / 0.17 h

2.2: 20 °C

3.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium carbonate / ethanol; water / 60 °C / Inert atmosphere

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; carbonochloridic acid 1-chloro-ethyl ester; sodium carbonate; potassium carbonate; In ethanol; water; 1,2-dichloro-ethane; acetonitrile;