4-(2-{2-[2-(Naphthalene-1-sulfonylamino)-acetylamino]-acetylamino}-3-oxo-3-pyrrolidin-1-yl-propyl)-thiobenzimidic acid methyl ester; hydriodide

Base Information

Chemical Name:4-(2-{2-[2-(Naphthalene-1-sulfonylamino)-acetylamino]-acetylamino}-3-oxo-3-pyrrolidin-1-yl-propyl)-thiobenzimidic acid methyl ester; hydriodide
CAS No.:93887-10-6
Molecular Formula:C₂₉H₃₃N₅O₅S₂*HI
Molecular Weight:723.656
Hs Code.:

4-(2-{2-[2-(Naphthalene-1-sulfonylamino)-acetylamino]-acetylamino}-3-oxo-3-pyrrolidin-1-yl-propyl)-thiobenzimidic acid methyl ester; hydriodide

Synonyms:4-(2-{2-[2-(Naphthalene-1-sulfonylamino)-acetylamino]-acetylamino}-3-oxo-3-pyrrolidin-1-yl-propyl)-thiobenzimidic acid methyl ester; hydriodide

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Chemical Property of 4-(2-{2-[2-(Naphthalene-1-sulfonylamino)-acetylamino]-acetylamino}-3-oxo-3-pyrrolidin-1-yl-propyl)-thiobenzimidic acid methyl ester; hydriodide

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Technology Process of 4-(2-{2-[2-(Naphthalene-1-sulfonylamino)-acetylamino]-acetylamino}-3-oxo-3-pyrrolidin-1-yl-propyl)-thiobenzimidic acid methyl ester; hydriodide

There total 8 articles about 4-(2-{2-[2-(Naphthalene-1-sulfonylamino)-acetylamino]-acetylamino}-3-oxo-3-pyrrolidin-1-yl-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: 60.0%

: 93886-98-7
2-(Naphthalene-1-sulfonylamino)-N-{[2-oxo-2-pyrrolidin-1-yl-1-(4-thiocarbamoyl-benzyl)-ethylcarbamoyl]-methyl}-acetamide

: 74-88-4
methyl iodide

: 93887-10-6
4-(2-{2-[2-(Naphthalene-1-sulfonylamino)-acetylamino]-acetylamino}-3-oxo-3-pyrrolidin-1-yl-propyl)-thiobenzimidic acid methyl ester; hydriodide

Guidance literature:: In acetone; for 0.166667h; Heating;

Reference yield:

: 92740-47-1
α-naphthylenesulfonylglycine

: 93887-10-6
4-(2-{2-[2-(Naphthalene-1-sulfonylamino)-acetylamino]-acetylamino}-3-oxo-3-pyrrolidin-1-yl-propyl)-thiobenzimidic acid methyl ester; hydriodide

Guidance literature:: Multi-step reaction with 8 steps

1: SOCl₂ / 1 h / Heating

2: 2 M NaOH / CHCl₃; ethyl acetate / 10 h

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

4: 75 percent / Et₃N / pyridine; ethyl acetate / 2 h

5: DCC / pyridine; ethyl acetate / 1.) 2 h, 2.) 10 h, room temperature

6: CHCl₃ / 2 h

7: 85 percent / H₂S, TEA / pyridine / Ambient temperature

8: 60 percent / acetone / 0.17 h / Heating

With sodium hydroxide; thionyl chloride; TEA; hydrogen sulfide; triethylamine; dicyclohexyl-carbodiimide; In pyridine; chloroform; ethyl acetate; acetone;

Reference yield:

: 93886-71-6
1-Naphthylsulfonylglycylglycin

: 93887-10-6
4-(2-{2-[2-(Naphthalene-1-sulfonylamino)-acetylamino]-acetylamino}-3-oxo-3-pyrrolidin-1-yl-propyl)-thiobenzimidic acid methyl ester; hydriodide

Guidance literature:: Multi-step reaction with 6 steps

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

2: 75 percent / Et₃N / pyridine; ethyl acetate / 2 h

3: DCC / pyridine; ethyl acetate / 1.) 2 h, 2.) 10 h, room temperature

4: CHCl₃ / 2 h

5: 85 percent / H₂S, TEA / pyridine / Ambient temperature

6: 60 percent / acetone / 0.17 h / Heating

With TEA; hydrogen sulfide; triethylamine; dicyclohexyl-carbodiimide; In pyridine; chloroform; ethyl acetate; acetone;