(R,E)-2,4-dihydroxy-3,3-dimethyl-N-(3-oxo-3-(4-(phenylsulfonyl)but-3-enylamino)propyl)-butanamide

Base Information

Chemical Name:(R,E)-2,4-dihydroxy-3,3-dimethyl-N-(3-oxo-3-(4-(phenylsulfonyl)but-3-enylamino)propyl)-butanamide
CAS No.:1245941-20-1
Molecular Formula:C₁₉H₂₈N₂O₆S
Molecular Weight:412.507
Hs Code.:

Synonyms:(R,E)-2,4-dihydroxy-3,3-dimethyl-N-(3-oxo-3-(4-(phenylsulfonyl)but-3-enylamino)propyl)-butanamide

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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 (R,E)-2,4-dihydroxy-3,3-dimethyl-N-(3-oxo-3-(4-(phenylsulfonyl)but-3-enylamino)propyl)-butanamide

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Technology Process of (R,E)-2,4-dihydroxy-3,3-dimethyl-N-(3-oxo-3-(4-(phenylsulfonyl)but-3-enylamino)propyl)-butanamide

There total 1 articles about (R,E)-2,4-dihydroxy-3,3-dimethyl-N-(3-oxo-3-(4-(phenylsulfonyl)but-3-enylamino)propyl)-butanamide 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: 64.0%

: 1256166-26-3
(E)-4-(phenylsulfonyl)but-3-en-1-amine hydrochloride

: 137-08-6
calcium (R)-pantothenate

: 1245941-20-1
(R,E)-2,4-dihydroxy-3,3-dimethyl-N-(3-oxo-3-(4-(phenylsulfonyl)but-3-enylamino)propyl)-butanamide

Guidance literature:: With N-ethylmorpholine;; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1021/ja106204m

Reference yield: 61.0%

: 1245941-20-1
(R,E)-2,4-dihydroxy-3,3-dimethyl-N-(3-oxo-3-(4-(phenylsulfonyl)but-3-enylamino)propyl)-butanamide

: 56-65-5,896506-78-8
ATP

: 1245941-25-6
C₂₉H₄₂N₇O₁₈P₃S

Guidance literature:: With pyruvate kinase; inorganic pyrophosphatase; Escherichia coli dephospho-CoA kinase; Staphylococcus aureus pantothenate kinase; phosphoenolpyruvic acid; magnesium chloride; Escherichia coli phosphopantetheine adenylyltransferase; at 37 ℃; for 18h; pH=7.6; aq. buffer; Enzymatic reaction;
DOI:10.1021/ja106204m