1-(4-aminophenyl)-3-cyclohexylmethyl-3-azabicyclo[-3.1.1]heptane-2,4-dione

Base Information

Chemical Name:1-(4-aminophenyl)-3-cyclohexylmethyl-3-azabicyclo[-3.1.1]heptane-2,4-dione
CAS No.:103297-83-2
Molecular Formula:C₁₉H₂₄N₂O₂
Molecular Weight:312.412
Hs Code.:

Synonyms:1-(4-aminophenyl)-3-cyclohexylmethyl-3-azabicyclo[-3.1.1]heptane-2,4-dione

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Chemical Property of 1-(4-aminophenyl)-3-cyclohexylmethyl-3-azabicyclo[-3.1.1]heptane-2,4-dione

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Technology Process of 1-(4-aminophenyl)-3-cyclohexylmethyl-3-azabicyclo[-3.1.1]heptane-2,4-dione

There total 5 articles about 1-(4-aminophenyl)-3-cyclohexylmethyl-3-azabicyclo[-3.1.1]heptane-2,4-dione 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: 51.0%

: 103297-84-3
3-cyclohexylmethyl-1-(4-nitrophenyl)-3-azabicyclo-[3.1.1]heptane-2,4-dione

: 103297-83-2
1-(4-aminophenyl)-3-cyclohexylmethyl-3-azabicyclo[-3.1.1]heptane-2,4-dione

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol;
DOI:10.1021/jm00108a013

Reference yield:

: 51747-44-5
α-(p-nitrophenyl)acrylic acid

: 103297-83-2
1-(4-aminophenyl)-3-cyclohexylmethyl-3-azabicyclo[-3.1.1]heptane-2,4-dione

Guidance literature:: Multi-step reaction with 4 steps

1: oxalyl chloride / CH₂Cl₂; dimethylformamide / 2 h / Ambient temperature

2: triethylamine / CH₂Cl₂ / 1.5 h / Ambient temperature

3: 42 percent / 2,6-di-tert-butyl-p-cresol / various solvent(s) / 1.5 h / 170 °C

4: 51 percent / H₂ / 5percent Pd/C / ethanol

With oxalyl dichloride; 2,6-di-tert-butyl-4-methyl-phenol; hydrogen; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00108a013

Reference yield:

: 103296-88-4
2-(4-Nitro-phenyl)-acryloyl chloride

: 103297-83-2
1-(4-aminophenyl)-3-cyclohexylmethyl-3-azabicyclo[-3.1.1]heptane-2,4-dione

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / CH₂Cl₂ / 1.5 h / Ambient temperature

2: 42 percent / 2,6-di-tert-butyl-p-cresol / various solvent(s) / 1.5 h / 170 °C

3: 51 percent / H₂ / 5percent Pd/C / ethanol

With 2,6-di-tert-butyl-4-methyl-phenol; hydrogen; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane;
DOI:10.1021/jm00108a013