methyl N-(3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-2-oxo-1,2-dihydropyridin-4-yl)phenyl)carbamate

Base Information

Chemical Name:methyl N-(3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-2-oxo-1,2-dihydropyridin-4-yl)phenyl)carbamate
CAS No.:1422388-52-0
Molecular Formula:C₂₂H₂₈N₄O₅
Molecular Weight:428.488
Hs Code.:

Synonyms:methyl N-(3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-2-oxo-1,2-dihydropyridin-4-yl)phenyl)carbamate

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Chemical Property of methyl N-(3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-2-oxo-1,2-dihydropyridin-4-yl)phenyl)carbamate

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Technology Process of methyl N-(3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-2-oxo-1,2-dihydropyridin-4-yl)phenyl)carbamate

There total 10 articles about methyl N-(3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-2-oxo-1,2-dihydropyridin-4-yl)phenyl)carbamate 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: 41.0%

: methyl N-(4-(6-(1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-2-oxo-1,2-dihydropyridin-4-yl)-3-nitrophenyl)carbamate

: 1422388-52-0
methyl N-(3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-2-oxo-1,2-dihydropyridin-4-yl)phenyl)carbamate

: 1422388-77-9
C₂₂H₂₈N₄O₅

Guidance literature:: With ammonium chloride; zinc; In methanol; at 20 - 65 ℃;

Reference yield:

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

: 1422388-52-0
methyl N-(3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-2-oxo-1,2-dihydropyridin-4-yl)phenyl)carbamate

: 1422388-77-9
C₂₂H₂₈N₄O₅

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium / tetrahydrofuran / -78 °C

1.2: -78 °C

2.1: potassium carbonate / tetrahydrofuran; ethanol / 0 - 55 °C / Inert atmosphere

3.1: ammonium acetate / ethanol / 75 °C

4.1: zinc; ammonium chloride / methanol / 20 - 65 °C

With n-butyllithium; ammonium acetate; potassium carbonate; ammonium chloride; zinc; In tetrahydrofuran; methanol; ethanol;

Reference yield:

: 773095-63-9
methyl 4-( 1,3-dioxolan-2-yl)-3-nitrobenzoate

: 1422388-52-0
methyl N-(3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-2-oxo-1,2-dihydropyridin-4-yl)phenyl)carbamate

: 1422388-77-9
C₂₂H₂₈N₄O₅

Guidance literature:: Multi-step reaction with 7 steps

1.1: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 1 h / 50 °C

2.1: chloroformic acid ethyl ester; triethylamine / tetrahydrofuran / 0.67 h / -5 °C

3.1: toluene / 1 h / 110 °C

3.2: 80 °C

4.1: water; trifluoroacetic acid / 3 h / 20 °C

5.1: potassium carbonate / tetrahydrofuran; ethanol / 0 - 55 °C / Inert atmosphere

6.1: ammonium acetate / ethanol / 75 °C

7.1: zinc; ammonium chloride / methanol / 20 - 65 °C

With lithium hydroxide monohydrate; ammonium acetate; water; chloroformic acid ethyl ester; potassium carbonate; ammonium chloride; triethylamine; trifluoroacetic acid; zinc; In tetrahydrofuran; methanol; ethanol; toluene;