(S)-methyl ((2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-5-guanidino)-2-((3-(4-nitro-benzenesulfonylamino)thiophene-2-carbonyl)amino))pentanoate

Base Information

Chemical Name:(S)-methyl ((2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-5-guanidino)-2-((3-(4-nitro-benzenesulfonylamino)thiophene-2-carbonyl)amino))pentanoate
CAS No.:1207974-51-3
Molecular Formula:C₃₁H₃₈N₆O₁₀S₃
Molecular Weight:750.875
Hs Code.:

(S)-methyl ((2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-5-guanidino)-2-((3-(4-nitro-benzenesulfonylamino)thiophene-2-carbonyl)amino))pentanoate

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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 (S)-methyl ((2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-5-guanidino)-2-((3-(4-nitro-benzenesulfonylamino)thiophene-2-carbonyl)amino))pentanoate

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Technology Process of (S)-methyl ((2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-5-guanidino)-2-((3-(4-nitro-benzenesulfonylamino)thiophene-2-carbonyl)amino))pentanoate

There total 1 articles about (S)-methyl ((2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-5-guanidino)-2-((3-(4-nitro-benzenesulfonylamino)thiophene-2-carbonyl)amino))pentanoate 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: 34.0%

: methyl N^ω-[(2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran-5-yl)sulfonyl]argininate

: C₁₁H₇N₂O₆PolS₂

: 1207974-51-3
(S)-methyl ((2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-5-guanidino)-2-((3-(4-nitro-benzenesulfonylamino)thiophene-2-carbonyl)amino))pentanoate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; for 3h; solid phase reaction;
DOI:10.1021/jm901755g