N-{[1-(4-Cyano-benzyl)-2-morpholin-4-yl-2-oxo-ethylcarbamoyl]-methyl}-2-(toluene-4-sulfonylamino)-acetamide

Base Information

Chemical Name:N-{[1-(4-Cyano-benzyl)-2-morpholin-4-yl-2-oxo-ethylcarbamoyl]-methyl}-2-(toluene-4-sulfonylamino)-acetamide
CAS No.:93886-80-7
Molecular Formula:C₂₅H₂₉N₅O₆S
Molecular Weight:527.601
Hs Code.:

Synonyms:N-{[1-(4-Cyano-benzyl)-2-morpholin-4-yl-2-oxo-ethylcarbamoyl]-methyl}-2-(toluene-4-sulfonylamino)-acetamide

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Chemical Property of N-{[1-(4-Cyano-benzyl)-2-morpholin-4-yl-2-oxo-ethylcarbamoyl]-methyl}-2-(toluene-4-sulfonylamino)-acetamide

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Technology Process of N-{[1-(4-Cyano-benzyl)-2-morpholin-4-yl-2-oxo-ethylcarbamoyl]-methyl}-2-(toluene-4-sulfonylamino)-acetamide

There total 6 articles about N-{[1-(4-Cyano-benzyl)-2-morpholin-4-yl-2-oxo-ethylcarbamoyl]-methyl}-2-(toluene-4-sulfonylamino)-acetamide 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:

: 4703-34-8
N-(p-tosyl)glycylglycine

: 93886-80-7
N-{[1-(4-Cyano-benzyl)-2-morpholin-4-yl-2-oxo-ethylcarbamoyl]-methyl}-2-(toluene-4-sulfonylamino)-acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: 70 percent / DCC / pyridine / 1.) 2 h, 2.) 10 h, room temperature

2: 60 percent / 1 M NaOH / pyridine; H₂O / 4 h

3: DCC / pyridine / 10 h / Ambient temperature

4: pyridine / 12 h

With sodium hydroxide; dicyclohexyl-carbodiimide; In pyridine; water;

Reference yield:

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

: 93886-80-7
N-{[1-(4-Cyano-benzyl)-2-morpholin-4-yl-2-oxo-ethylcarbamoyl]-methyl}-2-(toluene-4-sulfonylamino)-acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: 2 M NaOH / diethyl ether / 10 h

2: 70 percent / DCC / pyridine / 1.) 2 h, 2.) 10 h, room temperature

3: 60 percent / 1 M NaOH / pyridine; H₂O / 4 h

4: DCC / pyridine / 10 h / Ambient temperature

5: pyridine / 12 h

With sodium hydroxide; dicyclohexyl-carbodiimide; In pyridine; diethyl ether; water;

Reference yield:

: 1080-44-0
N-Tosylglycine

: 93886-80-7
N-{[1-(4-Cyano-benzyl)-2-morpholin-4-yl-2-oxo-ethylcarbamoyl]-methyl}-2-(toluene-4-sulfonylamino)-acetamide

Guidance literature:: Multi-step reaction with 6 steps

1: SOCl₂ / 1 h / Heating

2: 2 M NaOH / diethyl ether / 10 h

3: 70 percent / DCC / pyridine / 1.) 2 h, 2.) 10 h, room temperature

4: 60 percent / 1 M NaOH / pyridine; H₂O / 4 h

5: DCC / pyridine / 10 h / Ambient temperature

6: pyridine / 12 h

With sodium hydroxide; thionyl chloride; dicyclohexyl-carbodiimide; In pyridine; diethyl ether; water;