methyl (3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-3-chloropyridazin-4-yl)phenyl)carbamate

Base Information

Chemical Name:methyl (3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-3-chloropyridazin-4-yl)phenyl)carbamate
CAS No.:1422388-48-4
Molecular Formula:C₂₁H₂₆ClN₅O₄
Molecular Weight:447.922
Hs Code.:

Synonyms:methyl (3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-3-chloropyridazin-4-yl)phenyl)carbamate

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Chemical Property of methyl (3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-3-chloropyridazin-4-yl)phenyl)carbamate

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Technology Process of methyl (3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-3-chloropyridazin-4-yl)phenyl)carbamate

There total 10 articles about methyl (3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-3-chloropyridazin-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: 32.0%

: 1422387-26-5
methyl (4-(6-(1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-3-chloropyridazin-4-yl)-3-nitrophenyl)carbamate

: 1422388-48-4
methyl (3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-3-chloropyridazin-4-yl)phenyl)carbamate

Guidance literature:: With iron; acetic acid; In water; at 70 ℃; for 1h;

Reference yield:

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

: 1422388-48-4
methyl (3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-3-chloropyridazin-4-yl)phenyl)carbamate

Guidance literature:: Multi-step reaction with 6 steps

1.1: pyridine / dichloromethane / 3 h / 0 °C

2.1: triethylamine / dichloromethane / 0.33 h / 0 °C

3.1: potassium carbonate / ethanol / 2 h / 20 °C

3.2: 3 h

3.3: 96 h / 20 °C

4.1: hydrogenchloride / methanol; 1,4-dioxane / 6 h / 20 °C

4.2: 80 °C

5.1: triethylamine / dichloromethane / 0 - 20 °C

6.1: iron; acetic acid / water / 1 h / 70 °C

With pyridine; hydrogenchloride; iron; potassium carbonate; acetic acid; triethylamine; In 1,4-dioxane; methanol; ethanol; dichloromethane; water;

Reference yield:

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

: 1422388-48-4
methyl (3-amino-4-(6-((1S)-1-((tert-butoxycarbonyl)amino)but-3-en-1-yl)-3-chloropyridazin-4-yl)phenyl)carbamate

Guidance literature:: Multi-step reaction with 7 steps

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

1.2: 1 h / 20 °C

2.1: selenium(IV) oxide; pyridine / 60 °C / Inert atmosphere

3.1: triethylamine / dichloromethane / 0.33 h / 0 °C

4.1: potassium carbonate / ethanol / 2 h / 20 °C

4.2: 3 h

4.3: 96 h / 20 °C

5.1: hydrogenchloride / methanol; 1,4-dioxane / 6 h / 20 °C

5.2: 80 °C

6.1: triethylamine / dichloromethane / 0 - 20 °C

7.1: iron; acetic acid / water / 1 h / 70 °C

With pyridine; hydrogenchloride; selenium(IV) oxide; bis-triphenylphosphine-palladium(II) chloride; iron; potassium carbonate; acetic acid; triethylamine; In 1,4-dioxane; methanol; ethanol; dichloromethane; water; toluene;