(R)-methyl 2-(N-(9-fluorenylmethylcarbonyl-N-3,5-dichloro-2-hydroxy-4-methylphenylamino))-3-phenylpropanoate

Base Information

Chemical Name:(R)-methyl 2-(N-(9-fluorenylmethylcarbonyl-N-3,5-dichloro-2-hydroxy-4-methylphenylamino))-3-phenylpropanoate
CAS No.:921199-04-4
Molecular Formula:C₃₂H₂₇Cl₂NO₅
Molecular Weight:576.476
Hs Code.:

Synonyms:(R)-methyl 2-(N-(9-fluorenylmethylcarbonyl-N-3,5-dichloro-2-hydroxy-4-methylphenylamino))-3-phenylpropanoate

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Chemical Property of (R)-methyl 2-(N-(9-fluorenylmethylcarbonyl-N-3,5-dichloro-2-hydroxy-4-methylphenylamino))-3-phenylpropanoate

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Technology Process of (R)-methyl 2-(N-(9-fluorenylmethylcarbonyl-N-3,5-dichloro-2-hydroxy-4-methylphenylamino))-3-phenylpropanoate

There total 4 articles about (R)-methyl 2-(N-(9-fluorenylmethylcarbonyl-N-3,5-dichloro-2-hydroxy-4-methylphenylamino))-3-phenylpropanoate 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:

: C₂₂H₁₅O₃Cl₂N

: 921199-04-4
(R)-methyl 2-(N-(9-fluorenylmethylcarbonyl-N-3,5-dichloro-2-hydroxy-4-methylphenylamino))-3-phenylpropanoate

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / N,N-diisopropylethylamine; benzoylquinidine / tetrahydrofuran / 4 h / -78 °C

2: -78 °C

With benzoylquinidine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran;
DOI:10.1002/anie.200602801

Reference yield:

: 921198-87-0
9-fluorenylmethyl 3,5-dichloro-2-hydroxy-4-methylphenylcarbamate

: 921199-04-4
(R)-methyl 2-(N-(9-fluorenylmethylcarbonyl-N-3,5-dichloro-2-hydroxy-4-methylphenylamino))-3-phenylpropanoate

Guidance literature:: Multi-step reaction with 3 steps

1: Pb(OAc)4 / tetrahydrofuran / 0.08 h / -78 °C

2: 62 percent / N,N-diisopropylethylamine; benzoylquinidine / tetrahydrofuran / 4 h / -78 °C

3: -78 °C

With lead(IV) acetate; benzoylquinidine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran;
DOI:10.1002/anie.200602801

Reference yield:

: 645-45-4
hydrocinnamic acid chloride

: 921199-04-4
(R)-methyl 2-(N-(9-fluorenylmethylcarbonyl-N-3,5-dichloro-2-hydroxy-4-methylphenylamino))-3-phenylpropanoate

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / N,N-diisopropylethylamine; benzoylquinidine / tetrahydrofuran / 4 h / -78 °C

2: -78 °C

With benzoylquinidine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran;
DOI:10.1002/anie.200602801