3-[3-Morpholin-4-yl-3-oxo-2-(toluene-4-sulfonylamino)-propyl]-thiobenzimidic acid methyl ester; hydriodide

Base Information

Chemical Name:3-[3-Morpholin-4-yl-3-oxo-2-(toluene-4-sulfonylamino)-propyl]-thiobenzimidic acid methyl ester; hydriodide
CAS No.:80853-31-2
Molecular Formula:C₂₂H₂₇N₃O₄S₂*HI
Molecular Weight:589.519
Hs Code.:

Synonyms:3-[3-Morpholin-4-yl-3-oxo-2-(toluene-4-sulfonylamino)-propyl]-thiobenzimidic acid methyl ester; hydriodide

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Chemical Property of 3-[3-Morpholin-4-yl-3-oxo-2-(toluene-4-sulfonylamino)-propyl]-thiobenzimidic acid methyl ester; hydriodide

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Technology Process of 3-[3-Morpholin-4-yl-3-oxo-2-(toluene-4-sulfonylamino)-propyl]-thiobenzimidic acid methyl ester; hydriodide

There total 7 articles about 3-[3-Morpholin-4-yl-3-oxo-2-(toluene-4-sulfonylamino)-propyl]-thiobenzimidic acid methyl ester; 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: 48.0%

: 80852-95-5
3-[3-Morpholin-4-yl-3-oxo-2-(toluene-4-sulfonylamino)-propyl]-thiobenzamide

: 74-88-4
methyl iodide

: 80853-31-2
3-[3-Morpholin-4-yl-3-oxo-2-(toluene-4-sulfonylamino)-propyl]-thiobenzimidic acid methyl ester; hydriodide

Guidance literature:: In acetone; for 27h; Ambient temperature;

Reference yield:

: 52117-00-7
2-Acetylamino-2-[(3-cyanophenyl)-methyl]-malonic acid diethyl ester

: 80853-31-2
3-[3-Morpholin-4-yl-3-oxo-2-(toluene-4-sulfonylamino)-propyl]-thiobenzimidic acid methyl ester; hydriodide

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) 3 M HCl, 2.) 1 M KOH / 1.) acetic acid, 6 h, reflux, 2.) ether, 12 h, r.t.

2: SOCl₂ / 1 h / Heating

3: 83 percent / benzene / 1.5 h / Ambient temperature

4: 100 percent / H₂S (gas), TEA / pyridine / 72 h / Ambient temperature

5: 48 percent / acetone / 27 h / Ambient temperature

With hydrogenchloride; potassium hydroxide; thionyl chloride; TEA; hydrogen sulfide; In pyridine; acetone; benzene;

Reference yield:

: 98-59-9
p-toluenesulfonyl chloride

: 80853-31-2
3-[3-Morpholin-4-yl-3-oxo-2-(toluene-4-sulfonylamino)-propyl]-thiobenzimidic acid methyl ester; hydriodide

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) 3 M HCl, 2.) 1 M KOH / 1.) acetic acid, 6 h, reflux, 2.) ether, 12 h, r.t.

2: SOCl₂ / 1 h / Heating

3: 83 percent / benzene / 1.5 h / Ambient temperature

4: 100 percent / H₂S (gas), TEA / pyridine / 72 h / Ambient temperature

5: 48 percent / acetone / 27 h / Ambient temperature

With hydrogenchloride; potassium hydroxide; thionyl chloride; TEA; hydrogen sulfide; In pyridine; acetone; benzene;