5-guanidino-2(S)-[3-(1-methyl-1-phenylethyl)benzenesulfonylamino]pentanoic acid

Base Information

Chemical Name:5-guanidino-2(S)-[3-(1-methyl-1-phenylethyl)benzenesulfonylamino]pentanoic acid
CAS No.:154938-96-2
Molecular Formula:C₂₁H₂₈N₄O₄S
Molecular Weight:432.544
Hs Code.:

Synonyms:5-guanidino-2(S)-[3-(1-methyl-1-phenylethyl)benzenesulfonylamino]pentanoic acid

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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 5-guanidino-2(S)-[3-(1-methyl-1-phenylethyl)benzenesulfonylamino]pentanoic acid

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Technology Process of 5-guanidino-2(S)-[3-(1-methyl-1-phenylethyl)benzenesulfonylamino]pentanoic acid

There total 3 articles about 5-guanidino-2(S)-[3-(1-methyl-1-phenylethyl)benzenesulfonylamino]pentanoic acid 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: 83.0%

: 74-79-3,25212-18-4
L-arginine

: 154938-95-1
3-(1-methyl-1-phenylethyl)benzenesulfonyl chloride

: 154938-96-2
5-guanidino-2(S)-[3-(1-methyl-1-phenylethyl)benzenesulfonylamino]pentanoic acid

Guidance literature:: With potassium carbonate; In 1,4-dioxane; water; at 20 ℃; for 2h;
DOI:10.1021/jm9811209

Reference yield:

: 74-79-3,25212-18-4
L-arginine

: 584-08-7
potassium carbonate

: 154938-95-1
3-(1-methyl-1-phenylethyl)benzenesulfonyl chloride

: 154938-96-2
5-guanidino-2(S)-[3-(1-methyl-1-phenylethyl)benzenesulfonylamino]pentanoic acid

Guidance literature:: In 1,4-dioxane; water;

Reference yield:

: sodium 3-(1-methyl-1-phenylethyl)benzenesulfonate

: 154938-96-2
5-guanidino-2(S)-[3-(1-methyl-1-phenylethyl)benzenesulfonylamino]pentanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / thionyl chloride / dimethylformamide / 1 h / 20 °C

2: 83 percent / K₂CO₃ / H₂O; dioxane / 2 h / 20 °C

With thionyl chloride; potassium carbonate; In 1,4-dioxane; water; N,N-dimethyl-formamide; 1: Chlorination / 2: sulfonylation;
DOI:10.1021/jm9811209