(2-R,E)-N-4'-((3''-fluoro)styryl)benzyl 2-acetamido-3-methoxypropionamide

Base Information

Chemical Name:(2-R,E)-N-4'-((3''-fluoro)styryl)benzyl 2-acetamido-3-methoxypropionamide
CAS No.:1226775-87-6
Molecular Formula:C₂₁H₂₃FN₂O₃
Molecular Weight:370.424
Hs Code.:

Synonyms:(2-R,E)-N-4'-((3''-fluoro)styryl)benzyl 2-acetamido-3-methoxypropionamide

Suppliers and Price of (2-R,E)-N-4'-((3''-fluoro)styryl)benzyl 2-acetamido-3-methoxypropionamide

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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 (2-R,E)-N-4'-((3''-fluoro)styryl)benzyl 2-acetamido-3-methoxypropionamide

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Technology Process of (2-R,E)-N-4'-((3''-fluoro)styryl)benzyl 2-acetamido-3-methoxypropionamide

There total 1 articles about (2-R,E)-N-4'-((3''-fluoro)styryl)benzyl 2-acetamido-3-methoxypropionamide 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: 37.0%

: 849062-22-2
(E)-2-(3’-fluoro)phenylethenylboronic acid

: 1192590-80-9
(R)-N-4'-(iodo)benzyl 2-acetamido-3-methoxypropionamide

: 1226775-87-6
(2-R,E)-N-4'-((3''-fluoro)styryl)benzyl 2-acetamido-3-methoxypropionamide

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; caesium carbonate; In 1,4-dioxane; water; for 16h; Inert atmosphere; Reflux;
DOI:10.1021/jm100185c

Reference yield: 94.0%

: 1226775-87-6
(2-R,E)-N-4'-((3''-fluoro)styryl)benzyl 2-acetamido-3-methoxypropionamide

: 1197982-81-2
(R)-N-4'-((3''-fluoro)phenethyl)benzyl 2-acetamido-3-methoxypropionamide

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In ethanol; at 20 ℃; for 36h; under 760.051 Torr;
DOI:10.1021/jm100185c