N-allyl-2-nitro-N-(2-oxo-1-(S)-phenyl-2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide

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Chemical Name:N-allyl-2-nitro-N-(2-oxo-1-(S)-phenyl-2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide
CAS No.:777892-62-3
Molecular Formula:C₂₁H₂₃N₃O₅S
Molecular Weight:429.497
Hs Code.:

Synonyms:N-allyl-2-nitro-N-(2-oxo-1-(S)-phenyl-2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-allyl-2-nitro-N-(2-oxo-1-(S)-phenyl-2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide

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Technology Process of N-allyl-2-nitro-N-(2-oxo-1-(S)-phenyl-2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide

There total 4 articles about N-allyl-2-nitro-N-(2-oxo-1-(S)-phenyl-2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide 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: 96.2%

: 106-95-6
allyl bromide

: 777892-60-1
2-nitro-N-(2-oxo-1-(S)-phenyl-2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide

: 777892-62-3
N-allyl-2-nitro-N-(2-oxo-1-(S)-phenyl-2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 25 ℃; for 16h;
DOI:10.1016/j.bmcl.2004.08.041

Reference yield:

: 2935-35-5
(S)-2-phenylglycine

: 777892-62-3
N-allyl-2-nitro-N-(2-oxo-1-(S)-phenyl-2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: aq. NaOH / 0.5 h / 25 °C

1.2: 85 percent / aq. NaOH / tetrahydrofuran / 20 h / 0 - 25 °C

2.1: 91 percent / HOBT; DCC / tetrahydrofuran; CH₂Cl₂ / 16 h / 0 - 25 °C

3.1: 96 percent / K₂CO₃ / dimethylformamide / 16 h / 25 °C

With sodium hydroxide; potassium carbonate; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 1.2: Fukuyama sulfonylation;
DOI:10.1016/j.bmcl.2004.08.041

Reference yield:

: 1694-92-4
2-Nitrobenzenesulfonyl chloride

: 777892-62-3
N-allyl-2-nitro-N-(2-oxo-1-(S)-phenyl-2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: aq. NaOH / 0.5 h / 25 °C

1.2: 85 percent / aq. NaOH / tetrahydrofuran / 20 h / 0 - 25 °C

2.1: 91 percent / HOBT; DCC / tetrahydrofuran; CH₂Cl₂ / 16 h / 0 - 25 °C

3.1: 96 percent / K₂CO₃ / dimethylformamide / 16 h / 25 °C

With sodium hydroxide; potassium carbonate; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 1.2: Fukuyama sulfonylation;
DOI:10.1016/j.bmcl.2004.08.041