3-(benzoylamino)-3-(pentamethylenecarbamoyl)-1-(phenylsulfonyl)cyclobutane-1-carboxylic acid

Base Information

Chemical Name:3-(benzoylamino)-3-(pentamethylenecarbamoyl)-1-(phenylsulfonyl)cyclobutane-1-carboxylic acid
CAS No.:161181-44-8
Molecular Formula:C₂₄H₂₆N₂O₆S
Molecular Weight:470.546
Hs Code.:

Synonyms:3-(benzoylamino)-3-(pentamethylenecarbamoyl)-1-(phenylsulfonyl)cyclobutane-1-carboxylic acid

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Chemical Property of 3-(benzoylamino)-3-(pentamethylenecarbamoyl)-1-(phenylsulfonyl)cyclobutane-1-carboxylic acid

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Technology Process of 3-(benzoylamino)-3-(pentamethylenecarbamoyl)-1-(phenylsulfonyl)cyclobutane-1-carboxylic acid

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

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

: 161181-44-8
3-(benzoylamino)-3-(pentamethylenecarbamoyl)-1-(phenylsulfonyl)cyclobutane-1-carboxylic acid

Guidance literature:: Multi-step reaction with 4 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

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

Reference yield:

: 124291-40-3
3-Benzenesulfonyl-bicyclo[1.1.0]butane-1-carboxylic acid

: 161181-44-8
3-(benzoylamino)-3-(pentamethylenecarbamoyl)-1-(phenylsulfonyl)cyclobutane-1-carboxylic acid

Guidance literature:: Multi-step reaction with 7 steps

1: 92 percent / TMG, NaN₃ / dimethylformamide / 6 h / 90 °C

2: SOCl₂ / 1 h / 75 °C

3: CH₂Cl₂ / 1 h / Ambient temperature

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

5: 96 percent / Heating

6: Et₃N / 1 h / 0 - 20 °C

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

With n-butyllithium; thionyl chloride; sodium azide; hydrogen; triethylamine; N,N,N',N'-tetramethylguanidine; palladium on activated charcoal; In dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm00051a005

Reference yield:

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

: 161181-44-8
3-(benzoylamino)-3-(pentamethylenecarbamoyl)-1-(phenylsulfonyl)cyclobutane-1-carboxylic acid

Guidance literature:: Multi-step reaction with 5 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

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