tert-Butyl 2-(5-bromo-2-(2-hydroxyethylamino)phenylamino)-2-oxoethylcarbamate

Base Information

Chemical Name:tert-Butyl 2-(5-bromo-2-(2-hydroxyethylamino)phenylamino)-2-oxoethylcarbamate
CAS No.:1382805-14-2
Molecular Formula:C₁₅H₂₂BrN₃O₄
Molecular Weight:388.261
Hs Code.:

Synonyms:tert-Butyl 2-(5-bromo-2-(2-hydroxyethylamino)phenylamino)-2-oxoethylcarbamate

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Chemical Property of tert-Butyl 2-(5-bromo-2-(2-hydroxyethylamino)phenylamino)-2-oxoethylcarbamate

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Technology Process of tert-Butyl 2-(5-bromo-2-(2-hydroxyethylamino)phenylamino)-2-oxoethylcarbamate

There total 2 articles about tert-Butyl 2-(5-bromo-2-(2-hydroxyethylamino)phenylamino)-2-oxoethylcarbamate 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:

: 4530-20-5
BOC-glycine

: 90002-50-9
2-(2-amino-4-bromophenylamino)ethanol

: 1382805-14-2
tert-Butyl 2-(5-bromo-2-(2-hydroxyethylamino)phenylamino)-2-oxoethylcarbamate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In dichloromethane; for 0.333333h;

Reference yield:

: 89980-83-6
2-(4-bromo-2-nitro-anilino)-ethanol

: 1382805-14-2
tert-Butyl 2-(5-bromo-2-(2-hydroxyethylamino)phenylamino)-2-oxoethylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: ammonium chloride; iron / ethanol; water / 2 h / 85 °C

2: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane / 0.33 h

With iron; ammonium chloride; N-ethyl-N,N-diisopropylamine; HATU; In ethanol; dichloromethane; water;

Reference yield:

: 1382805-14-2
tert-Butyl 2-(5-bromo-2-(2-hydroxyethylamino)phenylamino)-2-oxoethylcarbamate

: 1382805-19-7
tert-Butyl 8-(4-(benzyloxy)-2-oxopyridin-1(2H)-yl)-3,4-dihydropyrazino[1,2-a]benzimidazole-2(1H)-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride / dichloromethane; water / 2 h / 120 °C

2.1: potassium carbonate / isopropyl alcohol; water / 16 h

3.1: triethylamine / dichloromethane / 2 h

4.1: trifluoroacetic acid / trifluoroacetic acid / 1 h

4.2: 2 h / 105 °C

4.3: 48 h / 20 °C

5.1: caesium carbonate; copper(l) iodide; trans-N,N'-dimethyl-1,2-cyclohexyldiamine / 1,4-dioxane / 16 h / 110 °C / Inert atmosphere

With trans-N,N'-dimethyl-1,2-cyclohexyldiamine; hydrogenchloride; copper(l) iodide; potassium carbonate; caesium carbonate; triethylamine; trifluoroacetic acid; In 1,4-dioxane; dichloromethane; water; isopropyl alcohol; trifluoroacetic acid;