(S)-N-(3-(4-aminophenyl)-1-((2-hydroxyphenyl)amino)-1-oxopropan-2-yl)-2-hydroxybenzamide

Base Information

Chemical Name:(S)-N-(3-(4-aminophenyl)-1-((2-hydroxyphenyl)amino)-1-oxopropan-2-yl)-2-hydroxybenzamide
CAS No.:1373883-31-8
Molecular Formula:C₂₂H₂₁N₃O₄
Molecular Weight:391.426
Hs Code.:

Synonyms:(S)-N-(3-(4-aminophenyl)-1-((2-hydroxyphenyl)amino)-1-oxopropan-2-yl)-2-hydroxybenzamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S)-N-(3-(4-aminophenyl)-1-((2-hydroxyphenyl)amino)-1-oxopropan-2-yl)-2-hydroxybenzamide

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Technology Process of (S)-N-(3-(4-aminophenyl)-1-((2-hydroxyphenyl)amino)-1-oxopropan-2-yl)-2-hydroxybenzamide

There total 6 articles about (S)-N-(3-(4-aminophenyl)-1-((2-hydroxyphenyl)amino)-1-oxopropan-2-yl)-2-hydroxybenzamide 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: 97.0%

: 1373883-30-7
(S)-2-hydroxy-N-(1-((2-hydroxyphenyl)amino)-3-(4-nitrophenyl)-1-oxopropan-2-yl)benzamide

: 1373883-31-8
(S)-N-(3-(4-aminophenyl)-1-((2-hydroxyphenyl)amino)-1-oxopropan-2-yl)-2-hydroxybenzamide

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; dichloromethane; at 20 ℃; for 16h;
DOI:10.1002/anie.201106832

Reference yield:

: 1373883-27-2
(S)-tert-butyl (1-((2-methoxyphenyl)amino)-3-(4-nitrophenyl)-1-oxopropan-2-yl)carbamate

: 1373883-31-8
(S)-N-(3-(4-aminophenyl)-1-((2-hydroxyphenyl)amino)-1-oxopropan-2-yl)-2-hydroxybenzamide

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogenchloride / dichloromethane; cyclopentyl methyl ether / 24 h / 0 - 20 °C

2: triethylamine / dichloromethane / 0.25 h / 0 - 20 °C

3: boron tribromide / dichloromethane / 1 h / -78 - 0 °C

4: palladium 10% on activated carbon; hydrogen / methanol; dichloromethane / 16 h / 20 °C

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; boron tribromide; triethylamine; In methanol; dichloromethane; cyclopentyl methyl ether;
DOI:10.1002/anie.201106832

Reference yield:

: 1373883-29-4
(S)-2-methoxy-N-(1-((2-methoxyphenyl)amino)-3-(4-nitrophenyl)-1-oxopropan-2-yl)benzamide

: 1373883-31-8
(S)-N-(3-(4-aminophenyl)-1-((2-hydroxyphenyl)amino)-1-oxopropan-2-yl)-2-hydroxybenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: boron tribromide / dichloromethane / 1 h / -78 - 0 °C

2: palladium 10% on activated carbon; hydrogen / methanol; dichloromethane / 16 h / 20 °C

With palladium 10% on activated carbon; hydrogen; boron tribromide; In methanol; dichloromethane;
DOI:10.1002/anie.201106832