4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-benzamidine; hydriodide

Base Information

Chemical Name:4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-benzamidine; hydriodide
CAS No.:83101-86-4
Molecular Formula:C₂₇H₃₂N₄O₃S*HI
Molecular Weight:620.555
Hs Code.:

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

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

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

There total 9 articles about 4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-benzamidine; 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: 66.5%

: 83101-73-9
4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-thiobenzimidic acid methyl ester; hydriodide

: 83101-86-4
4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-benzamidine; hydriodide

Guidance literature:: With ammonium acetate; In ethanol; for 2.5h; Heating;

Reference yield:

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

: 83101-86-4
4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-benzamidine; hydriodide

Guidance literature:: Multi-step reaction with 8 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

7: 68.5 percent / acetone / Ambient temperature

8: 66.5 percent / 1.1M AcONH₄ / ethanol / 2.5 h / Heating

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

Reference yield:

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

: 83101-86-4
4-[4-(Naphthalene-1-sulfonylamino)-5-oxo-5-piperidin-1-yl-pentyl]-benzamidine; hydriodide

Guidance literature:: Multi-step reaction with 9 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

8: 68.5 percent / acetone / Ambient temperature

9: 66.5 percent / 1.1M AcONH₄ / ethanol / 2.5 h / Heating

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