2-{4-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-vinyl]-phenylsulfanyl}-2-methyl-propionic acid tert-butyl ester

Base Information

• Chemical Name: 2-{4-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-vinyl]-phenylsulfanyl}-2-methyl-propionic acid tert-butyl ester
• CAS No.: 265129-65-5
• Molecular Formula: C₂₄H₂₅NO₄S
• Molecular Weight: 423.533

Synonyms:2-{4-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-vinyl]-phenylsulfanyl}-2-methyl-propionic acid tert-butyl ester

Chemical Property of 2-{4-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-vinyl]-phenylsulfanyl}-2-methyl-propionic acid tert-butyl ester

Chemical Property:

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Technology Process of 2-{4-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-vinyl]-phenylsulfanyl}-2-methyl-propionic acid tert-butyl ester

There total 3 articles about 2-{4-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-vinyl]-phenylsulfanyl}-2-methyl-propionic acid tert-butyl ester 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: 84.0%

N-vinylphthalimide (3485-84-5,26809-43-8) + 1,1-dimethylethyl 2-[(4-bromophenyl)thio]-2-methyl-propanoate (247923-30-4) → 2-{4-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-vinyl]-phenylsulfanyl}-2-methyl-propionic acid tert-butyl ester (265129-65-5)

Guidance literature:

With palladium diacetate; N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine; In acetonitrile;

DOI:10.1021/jm9903601

Reference yield:

tert-butyl bromoisobutyrate (23877-12-5) → 2-{4-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-vinyl]-phenylsulfanyl}-2-methyl-propionic acid tert-butyl ester (265129-65-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 80 percent / KOH / ethanol

2: 84 percent / Pd(OAc)2; DIEA; (o-tol)3P / acetonitrile

With palladium diacetate; potassium hydroxide; N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine; In ethanol; acetonitrile; 1: Alkylation / 2: Substitution;

DOI:10.1021/jm9903601

Reference yield:

para-bromobenzenethiol (106-53-6) → 2-{4-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-vinyl]-phenylsulfanyl}-2-methyl-propionic acid tert-butyl ester (265129-65-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 80 percent / KOH / ethanol

2: 84 percent / Pd(OAc)2; DIEA; (o-tol)3P / acetonitrile

With palladium diacetate; potassium hydroxide; N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine; In ethanol; acetonitrile; 1: Alkylation / 2: Substitution;

DOI:10.1021/jm9903601

upstream raw materials:

N-vinylphthalimide

1,1-dimethylethyl 2-[(4-bromophenyl)thio]-2-methyl-propanoate

tert-butyl bromoisobutyrate

para-bromobenzenethiol

Downstream raw materials:

t-Butyl 2-(4-(2-(1-Heptyl-3-(2,4-difluorophenyl)ureido)ethyl)phenylthio)-2-methylpropionate

t-Butyl N-Heptanoyl-2-(4-(2-aminoethyl)phenylthio)-2-methylpropionate

1,1-dimethylethyl 2-[[4-(2-aminoethyl)phenyl]thio]-2-methyl-propanoate

2-{4-[2-(1,3-dioxo-1,3-dihydroisoindol-2-yl)ethyl]pheylsulfanyl}-2-methylpropionic acid tert-butyl ester

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