trans-1-(benzoylamino)-1-(pentamethylenecarbamoyl)cyclobutane-3-carboxylate

Base Information

Chemical Name:trans-1-(benzoylamino)-1-(pentamethylenecarbamoyl)cyclobutane-3-carboxylate
CAS No.:161181-48-2
Molecular Formula:C₁₈H₂₂N₂O₄
Molecular Weight:330.384
Hs Code.:

Synonyms:trans-1-(benzoylamino)-1-(pentamethylenecarbamoyl)cyclobutane-3-carboxylate

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Chemical Property of trans-1-(benzoylamino)-1-(pentamethylenecarbamoyl)cyclobutane-3-carboxylate

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Technology Process of trans-1-(benzoylamino)-1-(pentamethylenecarbamoyl)cyclobutane-3-carboxylate

There total 8 articles about trans-1-(benzoylamino)-1-(pentamethylenecarbamoyl)cyclobutane-3-carboxylate 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:

: 117488-02-5
cis-1-Azido-N,N-pentamethylene-3-(phenylsulfonyl)cyclobutane-1-carboxamide

: 161181-48-2
trans-1-(benzoylamino)-1-(pentamethylenecarbamoyl)cyclobutane-3-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: H₂ / Pd/C / ethyl acetate / 20 h / 760 Torr

2: 96 percent / Heating

3: Et₃N / 1 h / 0 - 20 °C

4: 1.) BuLi / 1.) THF, -40 deg C - -50 deg C, 1 h, 2.) THF, -50 deg C, - RT

5: 1.5 g / sodium amalgam / tetrahydrofuran; methanol / 3 h / Ambient temperature

With sodium amalgam; n-butyllithium; hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; ethyl acetate;
DOI:10.1021/jm00051a005

Reference yield:

: 161181-43-7
1-Azido-3-benzenesulfonyl-cyclobutanecarbonyl chloride

: 161181-48-2
trans-1-(benzoylamino)-1-(pentamethylenecarbamoyl)cyclobutane-3-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: CH₂Cl₂ / 1 h / Ambient temperature

2: H₂ / Pd/C / ethyl acetate / 20 h / 760 Torr

3: 96 percent / Heating

4: Et₃N / 1 h / 0 - 20 °C

5: 1.) BuLi / 1.) THF, -40 deg C - -50 deg C, 1 h, 2.) THF, -50 deg C, - RT

6: 1.5 g / sodium amalgam / tetrahydrofuran; methanol / 3 h / Ambient temperature

With sodium amalgam; n-butyllithium; hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate;
DOI:10.1021/jm00051a005

Reference yield:

: 117488-20-7
cis-1-Azido-3-(phenylsulfonyl)cyclobutane-1-carboxylic acid

: 161181-48-2
trans-1-(benzoylamino)-1-(pentamethylenecarbamoyl)cyclobutane-3-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1: SOCl₂ / 1 h / 75 °C

2: CH₂Cl₂ / 1 h / Ambient temperature

3: H₂ / Pd/C / ethyl acetate / 20 h / 760 Torr

4: 96 percent / Heating

5: Et₃N / 1 h / 0 - 20 °C

6: 1.) BuLi / 1.) THF, -40 deg C - -50 deg C, 1 h, 2.) THF, -50 deg C, - RT

7: 1.5 g / sodium amalgam / tetrahydrofuran; methanol / 3 h / Ambient temperature

With sodium amalgam; n-butyllithium; thionyl chloride; hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate;
DOI:10.1021/jm00051a005