N-[1-(4-Carbamimidoyl-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-2-(toluene-4-sulfonylamino)-acetamide; hydriodide

Base Information

Chemical Name:N-[1-(4-Carbamimidoyl-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-2-(toluene-4-sulfonylamino)-acetamide; hydriodide
CAS No.:84792-53-0
Molecular Formula:C₂₄H₃₁N₅O₄S*HI
Molecular Weight:613.52
Hs Code.:

Synonyms:N-[1-(4-Carbamimidoyl-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-2-(toluene-4-sulfonylamino)-acetamide; hydriodide

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Chemical Property of N-[1-(4-Carbamimidoyl-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-2-(toluene-4-sulfonylamino)-acetamide; hydriodide

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Technology Process of N-[1-(4-Carbamimidoyl-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-2-(toluene-4-sulfonylamino)-acetamide; hydriodide

There total 9 articles about N-[1-(4-Carbamimidoyl-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-2-(toluene-4-sulfonylamino)-acetamide; hydriodide 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: 73.0%

: 84792-51-8
4-{3-Oxo-3-piperidin-1-yl-2-[2-(toluene-4-sulfonylamino)-acetylamino]-propyl}-thiobenzimidic acid methyl ester; hydriodide

: 84792-53-0
N-[1-(4-Carbamimidoyl-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-2-(toluene-4-sulfonylamino)-acetamide; hydriodide

Guidance literature:: With ammonium acetate; In methanol; at 60 ℃; for 2.5h;

Reference yield:

: 52117-01-8
N-acetyl-4-cyano-α-(ethoxycarbonyl)phenylalanine ethyl ester

: 84792-53-0
N-[1-(4-Carbamimidoyl-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-2-(toluene-4-sulfonylamino)-acetamide; hydriodide

Guidance literature:: Multi-step reaction with 7 steps

1: NaOH (1 mol/l) / acetic acid; H₂O / pH 3.8-4.0

2: NaOH (1 mol/l) / diethyl ether; ethyl acetate; H₂O / 10 h

3: 60 percent / DCC / pyridine / 12 h / Ambient temperature

4: 40 percent / pyridine; dimethylformamide / 7 h / Ambient temperature

5: 62 percent / H₂S, TEA / pyridine / 72 h / Ambient temperature

6: 55 percent / acetone / 0.17 h / Heating

7: 73 percent / CH₃COONH₄ / methanol / 2.5 h / 60 °C

With sodium hydroxide; TEA; hydrogen sulfide; ammonium acetate; dicyclohexyl-carbodiimide; In pyridine; methanol; diethyl ether; water; acetic acid; ethyl acetate; N,N-dimethyl-formamide; acetone;

Reference yield:

: 56218-62-3
2-(4-methylphenylsulfonamido)acetyl chloride

: 84792-53-0
N-[1-(4-Carbamimidoyl-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-2-(toluene-4-sulfonylamino)-acetamide; hydriodide

Guidance literature:: Multi-step reaction with 6 steps

1: NaOH (1 mol/l) / diethyl ether; ethyl acetate; H₂O / 10 h

2: 60 percent / DCC / pyridine / 12 h / Ambient temperature

3: 40 percent / pyridine; dimethylformamide / 7 h / Ambient temperature

4: 62 percent / H₂S, TEA / pyridine / 72 h / Ambient temperature

5: 55 percent / acetone / 0.17 h / Heating

6: 73 percent / CH₃COONH₄ / methanol / 2.5 h / 60 °C

With sodium hydroxide; TEA; hydrogen sulfide; ammonium acetate; dicyclohexyl-carbodiimide; In pyridine; methanol; diethyl ether; water; ethyl acetate; N,N-dimethyl-formamide; acetone;