((S)-3-Benzenesulfonylamino-2-oxo-piperidin-1-yl)-acetic acid methyl ester

Base Information

Chemical Name:((S)-3-Benzenesulfonylamino-2-oxo-piperidin-1-yl)-acetic acid methyl ester
CAS No.:186261-79-0
Molecular Formula:C₁₄H₁₈N₂O₅S
Molecular Weight:326.373
Hs Code.:

Synonyms:((S)-3-Benzenesulfonylamino-2-oxo-piperidin-1-yl)-acetic acid methyl ester

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Chemical Property of ((S)-3-Benzenesulfonylamino-2-oxo-piperidin-1-yl)-acetic acid methyl ester

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Technology Process of ((S)-3-Benzenesulfonylamino-2-oxo-piperidin-1-yl)-acetic acid methyl ester

There total 8 articles about ((S)-3-Benzenesulfonylamino-2-oxo-piperidin-1-yl)-acetic acid methyl ester 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:

: 2480-93-5
Boc-Orn(Z)-OH

: 186261-79-0
((S)-3-Benzenesulfonylamino-2-oxo-piperidin-1-yl)-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 100 percent / H₂, AcOH / Pd/C / methanol; H₂O / 1810.02 - 2585.7 Torr

2: 80 percent / EDC, HOBt, NMM / acetonitrile / Ambient temperature

3: 85 percent / LiHMDS / tetrahydrofuran / Ambient temperature

4: 100 percent / H₂ / Pd/C / ethanol / 1551.4 Torr

5: 100 percent / HCl / 0 - 20 °C

6: Et₃N / acetonitrile / 0 - 20 °C

With 4-methyl-morpholine; hydrogenchloride; hydrogen; benzotriazol-1-ol; acetic acid; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; lithium hexamethyldisilazane; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; water; acetonitrile;
DOI:10.1021/jm960572n

Reference yield:

: 21887-64-9
N₂-(tert-butoxycarbonyl)-L-ornithine

: 186261-79-0
((S)-3-Benzenesulfonylamino-2-oxo-piperidin-1-yl)-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 80 percent / EDC, HOBt, NMM / acetonitrile / Ambient temperature

2: 85 percent / LiHMDS / tetrahydrofuran / Ambient temperature

3: 100 percent / H₂ / Pd/C / ethanol / 1551.4 Torr

4: 100 percent / HCl / 0 - 20 °C

5: Et₃N / acetonitrile / 0 - 20 °C

With 4-methyl-morpholine; hydrogenchloride; hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; lithium hexamethyldisilazane; palladium on activated charcoal; In tetrahydrofuran; ethanol; acetonitrile;
DOI:10.1021/jm960572n

Reference yield:

: 92235-39-7
3(S)-<(butoxycarbonyl)amino>-2-oxopiperidine

: 186261-79-0
((S)-3-Benzenesulfonylamino-2-oxo-piperidin-1-yl)-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 85 percent / LiHMDS / tetrahydrofuran / Ambient temperature

2: 100 percent / H₂ / Pd/C / ethanol / 1551.4 Torr

3: 100 percent / HCl / 0 - 20 °C

4: Et₃N / acetonitrile / 0 - 20 °C

With hydrogenchloride; hydrogen; triethylamine; lithium hexamethyldisilazane; palladium on activated charcoal; In tetrahydrofuran; ethanol; acetonitrile;
DOI:10.1021/jm960572n