methyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-(4-methoxyphenyl)pentanoate

Base Information

Chemical Name:methyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-(4-methoxyphenyl)pentanoate
CAS No.:303139-00-6
Molecular Formula:C₁₈H₂₇NO₅
Molecular Weight:337.416
Hs Code.:

Synonyms:methyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-(4-methoxyphenyl)pentanoate

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Chemical Property of methyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-(4-methoxyphenyl)pentanoate

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Technology Process of methyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-(4-methoxyphenyl)pentanoate

There total 7 articles about methyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-(4-methoxyphenyl)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: 69.0%

: 1415464-72-0
C₁₈H₂₃NO₅

: 303139-00-6
methyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-(4-methoxyphenyl)pentanoate

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; at 15 ℃; for 3h;

Reference yield: 60.0%

: 696-62-8
para-iodoanisole

: 89985-87-5
methyl (2S)-2-tert-butoxycarbonylamino-4-pentenoate

: 303139-00-6
methyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-(4-methoxyphenyl)pentanoate

Guidance literature:: methyl (2S)-2-tert-butoxycarbonylamino-4-pentenoate; With 9-borabicyclo[3.3.1]nonane dimer; In tetrahydrofuran; at 0 - 20 ℃; for 2h;

para-iodoanisole; With potassium phosphate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(00)01174-6

Reference yield:

: 696-62-8
para-iodoanisole

: 303139-00-6
methyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-(4-methoxyphenyl)pentanoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine / copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 0.5 h / 15 °C

1.2: 15 °C

2.1: hydrogen / palladium on activated charcoal / methanol / 3 h / 15 °C

With hydrogen; triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide;