N-Naphthalen-2-yl-3-(4-thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-propionamide

Base Information

Chemical Name:N-Naphthalen-2-yl-3-(4-thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-propionamide
CAS No.:80853-03-8
Molecular Formula:C₂₇H₂₅N₃O₃S₂
Molecular Weight:503.646
Hs Code.:

Synonyms:N-Naphthalen-2-yl-3-(4-thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-propionamide

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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-Naphthalen-2-yl-3-(4-thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-propionamide

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Technology Process of N-Naphthalen-2-yl-3-(4-thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-propionamide

There total 7 articles about N-Naphthalen-2-yl-3-(4-thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-propionamide 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: 95.0%

: 80852-67-1
3-(4-Cyano-phenyl)-N-naphthalen-2-yl-2-(toluene-4-sulfonylamino)-propionamide

: 80853-03-8
N-Naphthalen-2-yl-3-(4-thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-propionamide

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

Reference yield:

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

: 80853-03-8
N-Naphthalen-2-yl-3-(4-thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-propionamide

Guidance literature:: Multi-step reaction with 4 steps

2: SOCl₂ / 1 h / Heating

3: 100 percent / benzene / 1.5 h / Ambient temperature

4: 95 percent / H₂S (gas), TEA / pyridine / 72 h / Ambient temperature

With thionyl chloride; TEA; hydrogen sulfide; In pyridine; benzene;

Reference yield:

: 98-59-9
p-toluenesulfonyl chloride

: 80853-03-8
N-Naphthalen-2-yl-3-(4-thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-propionamide

Guidance literature:: Multi-step reaction with 4 steps

2: SOCl₂ / 1 h / Heating

3: 100 percent / benzene / 1.5 h / Ambient temperature

4: 95 percent / H₂S (gas), TEA / pyridine / 72 h / Ambient temperature

With thionyl chloride; TEA; hydrogen sulfide; In pyridine; benzene;