4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-thiobenzamide

Base Information

Chemical Name:4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-thiobenzamide
CAS No.:83101-60-4
Molecular Formula:C₂₇H₃₁N₃O₃S₂
Molecular Weight:509.693
Hs Code.:

Synonyms:4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-thiobenzamide

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Chemical Property of 4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-thiobenzamide

Chemical Property:

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Technology Process of 4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-thiobenzamide

There total 7 articles about 4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-thiobenzamide 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: 100.0%

: 83101-47-7
5-(4-Cyanphenyl)-2-α-naphthylsulfonylaminovaleriansaeurepiperidid

: 83101-60-4
4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-thiobenzamide

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

Reference yield:

: 35271-56-8,142917-82-6,1504-63-8
3-(4-nitrophenyl)propyl-2-en-1-ol

: 83101-60-4
4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-thiobenzamide

Guidance literature:: Multi-step reaction with 6 steps

1: 78 percent / H₂ / Raney-Ni / methanol / 760 Torr

2: 1.) HCl/NaNO₂ / 1.) H₂O; 2.) 0-5 deg C 30 min, room temp. 4 h

3: PBr₃ / CHCl₃ / 1.5 h / Heating

4: C₂H₂ONa / ethanol / 5 h / Heating

6: 100 percent / TEA, H₂S / pyridine / Ambient temperature

With hydrogenchloride; C₂H₂ONa; TEA; hydrogen sulfide; hydrogen; phosphorus tribromide; sodium nitrite; nickel; In pyridine; methanol; ethanol; chloroform;

Reference yield:

: 1734-79-8
3-(4-nitrophenyl)-2-propenal

: 83101-60-4
4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-thiobenzamide

Guidance literature:: Multi-step reaction with 7 steps

1: 70 percent / NaBH₄ / methanol

2: 78 percent / H₂ / Raney-Ni / methanol / 760 Torr

3: 1.) HCl/NaNO₂ / 1.) H₂O; 2.) 0-5 deg C 30 min, room temp. 4 h

4: PBr₃ / CHCl₃ / 1.5 h / Heating

5: C₂H₂ONa / ethanol / 5 h / Heating

7: 100 percent / TEA, H₂S / pyridine / Ambient temperature

With hydrogenchloride; sodium tetrahydroborate; C₂H₂ONa; TEA; hydrogen sulfide; hydrogen; phosphorus tribromide; sodium nitrite; nickel; In pyridine; methanol; ethanol; chloroform;