(S)-2-(4-(methoxycarbonylamino)-2-nitrophenyl)-2-oxoethyl 2-(tert-butoxycarbonylamino)pent-4-enoate

Base Information

Chemical Name:(S)-2-(4-(methoxycarbonylamino)-2-nitrophenyl)-2-oxoethyl 2-(tert-butoxycarbonylamino)pent-4-enoate
CAS No.:1422387-41-4
Molecular Formula:C₂₀H₂₅N₃O₉
Molecular Weight:451.433
Hs Code.:

Synonyms:(S)-2-(4-(methoxycarbonylamino)-2-nitrophenyl)-2-oxoethyl 2-(tert-butoxycarbonylamino)pent-4-enoate

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Chemical Property of (S)-2-(4-(methoxycarbonylamino)-2-nitrophenyl)-2-oxoethyl 2-(tert-butoxycarbonylamino)pent-4-enoate

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Technology Process of (S)-2-(4-(methoxycarbonylamino)-2-nitrophenyl)-2-oxoethyl 2-(tert-butoxycarbonylamino)pent-4-enoate

There total 5 articles about (S)-2-(4-(methoxycarbonylamino)-2-nitrophenyl)-2-oxoethyl 2-(tert-butoxycarbonylamino)pent-4-enoate 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: 100.0%

: 1329166-64-4
methyl (4-(2-bromoacetyl)-3-nitrophenyl)carbamate

: 90600-20-7
(2S)-2-[(tert-butoxycarbonyl)amino]pent-4-enoic acid

: 1422387-41-4
(S)-2-(4-(methoxycarbonylamino)-2-nitrophenyl)-2-oxoethyl 2-(tert-butoxycarbonylamino)pent-4-enoate

Guidance literature:: (2S)-2-[(tert-butoxycarbonyl)amino]pent-4-enoic acid; With potassium hydrogencarbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.333333h;

methyl (4-(2-bromoacetyl)-3-nitrophenyl)carbamate; In N,N-dimethyl-formamide; at 0 - 20 ℃;

Reference yield:

: 105752-04-3
3-nitro-4-iodoaniline

: 1422387-41-4
(S)-2-(4-(methoxycarbonylamino)-2-nitrophenyl)-2-oxoethyl 2-(tert-butoxycarbonylamino)pent-4-enoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: pyridine / dichloromethane / 1.5 h / 0 °C

2.1: bis-triphenylphosphine-palladium(II) chloride / toluene / 3 h / 110 °C / Sealed tube

2.2: 1 h / 20 °C

3.1: copper(ll) bromide / ethyl acetate / 3 h / 70 °C

4.1: potassium hydrogencarbonate / N,N-dimethyl-formamide / 0.33 h / 20 °C

4.2: 0 - 20 °C

With pyridine; bis-triphenylphosphine-palladium(II) chloride; potassium hydrogencarbonate; copper(ll) bromide; In dichloromethane; ethyl acetate; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1329166-65-5
methyl 4-iodo-3-nitrophenylcarbamate

: 1422387-41-4
(S)-2-(4-(methoxycarbonylamino)-2-nitrophenyl)-2-oxoethyl 2-(tert-butoxycarbonylamino)pent-4-enoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: bis-triphenylphosphine-palladium(II) chloride / toluene / 3 h / 110 °C / Sealed tube

1.2: 1 h / 20 °C

2.1: copper(ll) bromide / ethyl acetate / 3 h / 70 °C

3.1: potassium hydrogencarbonate / N,N-dimethyl-formamide / 0.33 h / 20 °C

3.2: 0 - 20 °C

With bis-triphenylphosphine-palladium(II) chloride; potassium hydrogencarbonate; copper(ll) bromide; In ethyl acetate; N,N-dimethyl-formamide; toluene;