5-(isoxazol-3-yl)thiophene-2-sulfonic acid [1-(2-amino-5-cyanobenzyl)-2-oxo-pyrrolidin-3-(S)-yl]amide

Base Information

Chemical Name:5-(isoxazol-3-yl)thiophene-2-sulfonic acid [1-(2-amino-5-cyanobenzyl)-2-oxo-pyrrolidin-3-(S)-yl]amide
CAS No.:245760-96-7
Molecular Formula:C₁₉H₁₇N₅O₄S₂
Molecular Weight:443.507
Hs Code.:

Synonyms:5-(isoxazol-3-yl)thiophene-2-sulfonic acid [1-(2-amino-5-cyanobenzyl)-2-oxo-pyrrolidin-3-(S)-yl]amide

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Chemical Property of 5-(isoxazol-3-yl)thiophene-2-sulfonic acid [1-(2-amino-5-cyanobenzyl)-2-oxo-pyrrolidin-3-(S)-yl]amide

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Technology Process of 5-(isoxazol-3-yl)thiophene-2-sulfonic acid [1-(2-amino-5-cyanobenzyl)-2-oxo-pyrrolidin-3-(S)-yl]amide

There total 7 articles about 5-(isoxazol-3-yl)thiophene-2-sulfonic acid [1-(2-amino-5-cyanobenzyl)-2-oxo-pyrrolidin-3-(S)-yl]amide 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:

: 4-amino-[3-(3-(S)-amino-2-oxo-pyrrolidin-1-ylmethyl)]-benzonitrile dihydrochloride

: 245760-96-7
5-(isoxazol-3-yl)thiophene-2-sulfonic acid [1-(2-amino-5-cyanobenzyl)-2-oxo-pyrrolidin-3-(S)-yl]amide

Guidance literature:: In 5-(isoxazol-3-yl)thiophen-2-sulfonyl chloride;

Reference yield:

: 96784-54-2
3-methyl-4-nitrobenzonitrile

: 245760-96-7
5-(isoxazol-3-yl)thiophene-2-sulfonic acid [1-(2-amino-5-cyanobenzyl)-2-oxo-pyrrolidin-3-(S)-yl]amide

Guidance literature:: Multi-step reaction with 6 steps

1.1: 96 percent / SnCl₂; EtOH / 2 h / Heating

2.1: 90 percent / p-toluenesulfonic acid / toluene / 24 h / Heating

3.1: 57 percent / N-bromosuccinimide; benzoyl peroxide / CCl₄ / 16 h / Heating

4.1: NaH / tetrahydrofuran; dimethylformamide / 0.08 h / 0 °C

4.2: 86 percent / tetrahydrofuran / 4 h / 0 °C

5.1: HCl / ethyl acetate / 1 h / 0 °C

6.1: Et₃N / acetonitrile / 5 h

With hydrogenchloride; N-Bromosuccinimide; ethanol; sodium hydride; toluene-4-sulfonic acid; triethylamine; tin(ll) chloride; dibenzoyl peroxide; In tetrahydrofuran; tetrachloromethane; ethyl acetate; N,N-dimethyl-formamide; toluene; acetonitrile; 1.1: Reduction / 2.1: Condensation / 3.1: Bromination / 4.1: Metallation / 4.2: Substitution / 5.1: Acidolysis / 6.1: Sulfonylation;
DOI:10.1021/jm990041+

Reference yield:

: 78881-21-7
4-amino-3-methylbenzonitrile

: 245760-96-7
5-(isoxazol-3-yl)thiophene-2-sulfonic acid [1-(2-amino-5-cyanobenzyl)-2-oxo-pyrrolidin-3-(S)-yl]amide

Guidance literature:: Multi-step reaction with 5 steps

1.1: 90 percent / p-toluenesulfonic acid / toluene / 24 h / Heating

2.1: 57 percent / N-bromosuccinimide; benzoyl peroxide / CCl₄ / 16 h / Heating

3.1: NaH / tetrahydrofuran; dimethylformamide / 0.08 h / 0 °C

3.2: 86 percent / tetrahydrofuran / 4 h / 0 °C

4.1: HCl / ethyl acetate / 1 h / 0 °C

5.1: Et₃N / acetonitrile / 5 h

With hydrogenchloride; N-Bromosuccinimide; sodium hydride; toluene-4-sulfonic acid; triethylamine; dibenzoyl peroxide; In tetrahydrofuran; tetrachloromethane; ethyl acetate; N,N-dimethyl-formamide; toluene; acetonitrile; 1.1: Condensation / 2.1: Bromination / 3.1: Metallation / 3.2: Substitution / 4.1: Acidolysis / 5.1: Sulfonylation;
DOI:10.1021/jm990041+