(S)-1-(Naphthalene-2-sulfonyl)-pyrrolidine-2-carboxylic acid [2-oxo-2-pyrrolidin-1-yl-1-(4-thiocarbamoyl-benzyl)-ethyl]-amide

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Chemical Name:(S)-1-(Naphthalene-2-sulfonyl)-pyrrolidine-2-carboxylic acid [2-oxo-2-pyrrolidin-1-yl-1-(4-thiocarbamoyl-benzyl)-ethyl]-amide
CAS No.:107994-21-8
Molecular Formula:C₂₉H₃₂N₄O₄S₂
Molecular Weight:564.729
Hs Code.:

Synonyms:(S)-1-(Naphthalene-2-sulfonyl)-pyrrolidine-2-carboxylic acid [2-oxo-2-pyrrolidin-1-yl-1-(4-thiocarbamoyl-benzyl)-ethyl]-amide

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Chemical Property of (S)-1-(Naphthalene-2-sulfonyl)-pyrrolidine-2-carboxylic acid [2-oxo-2-pyrrolidin-1-yl-1-(4-thiocarbamoyl-benzyl)-ethyl]-amide

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Technology Process of (S)-1-(Naphthalene-2-sulfonyl)-pyrrolidine-2-carboxylic acid [2-oxo-2-pyrrolidin-1-yl-1-(4-thiocarbamoyl-benzyl)-ethyl]-amide

There total 5 articles about (S)-1-(Naphthalene-2-sulfonyl)-pyrrolidine-2-carboxylic acid [2-oxo-2-pyrrolidin-1-yl-1-(4-thiocarbamoyl-benzyl)-ethyl]-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: 80.0%

: 107994-14-9
(S)-1-(Naphthalene-2-sulfonyl)-pyrrolidine-2-carboxylic acid [1-(4-cyano-benzyl)-2-oxo-2-pyrrolidin-1-yl-ethyl]-amide

: 107994-21-8
(S)-1-(Naphthalene-2-sulfonyl)-pyrrolidine-2-carboxylic acid [2-oxo-2-pyrrolidin-1-yl-1-(4-thiocarbamoyl-benzyl)-ethyl]-amide

Guidance literature:: With hydrogen sulfide; In pyridine; triethylamine; for 72h; Ambient temperature;

Reference yield:

: 91872-30-9
N-(2-naphthylsulfonyl)-(S)-proline

: 107994-21-8
(S)-1-(Naphthalene-2-sulfonyl)-pyrrolidine-2-carboxylic acid [2-oxo-2-pyrrolidin-1-yl-1-(4-thiocarbamoyl-benzyl)-ethyl]-amide

Guidance literature:: Multi-step reaction with 5 steps

1: DCC / pyridine / 2 h, 0 deg C; 12 h, room temp.

2: TEA / pyridine / 2 h

3: DCC / ethyl acetate; pyridine / 24 h / Ambient temperature

4: ethyl acetate; pyridine / 4 h / Ambient temperature

5: 80 percent / H₂S / pyridine; triethylamine / 72 h / Ambient temperature

With TEA; hydrogen sulfide; dicyclohexyl-carbodiimide; In pyridine; ethyl acetate; triethylamine;

Reference yield:

: (S)-1-(Naphthalene-2-sulfonyl)-pyrrolidine-2-carboxylic acid 4-nitro-phenyl ester

: 107994-21-8
(S)-1-(Naphthalene-2-sulfonyl)-pyrrolidine-2-carboxylic acid [2-oxo-2-pyrrolidin-1-yl-1-(4-thiocarbamoyl-benzyl)-ethyl]-amide

Guidance literature:: Multi-step reaction with 4 steps

1: TEA / pyridine / 2 h

2: DCC / ethyl acetate; pyridine / 24 h / Ambient temperature

3: ethyl acetate; pyridine / 4 h / Ambient temperature

4: 80 percent / H₂S / pyridine; triethylamine / 72 h / Ambient temperature

With TEA; hydrogen sulfide; dicyclohexyl-carbodiimide; In pyridine; ethyl acetate; triethylamine;