4-[(4-chloro-2-[(S)-hydroxy(2-methoxyphenyl)methyl]-6-methylphenyl)(2,2-dimethylpropyl)amino]-4-oxobutanoicacid

Base Information

Chemical Name:4-[(4-chloro-2-[(S)-hydroxy(2-methoxyphenyl)methyl]-6-methylphenyl)(2,2-dimethylpropyl)amino]-4-oxobutanoicacid
CAS No.:1334531-20-2
Molecular Formula:C₂₄H₃₀ClNO₅
Molecular Weight:447.959
Hs Code.:

Synonyms:4-[(4-chloro-2-[(S)-hydroxy(2-methoxyphenyl)methyl]-6-methylphenyl)(2,2-dimethylpropyl)amino]-4-oxobutanoicacid

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Chemical Property of 4-[(4-chloro-2-[(S)-hydroxy(2-methoxyphenyl)methyl]-6-methylphenyl)(2,2-dimethylpropyl)amino]-4-oxobutanoicacid

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Technology Process of 4-[(4-chloro-2-[(S)-hydroxy(2-methoxyphenyl)methyl]-6-methylphenyl)(2,2-dimethylpropyl)amino]-4-oxobutanoicacid

There total 7 articles about 4-[(4-chloro-2-[(S)-hydroxy(2-methoxyphenyl)methyl]-6-methylphenyl)(2,2-dimethylpropyl)amino]-4-oxobutanoicacid 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: 92.0%

: 1334531-19-9
methyl 4-[(4-chloro-2-[(S)-hydroxy(2-methoxyphenyl)methyl]-6-methylphenyl)(2,2-dimethylpropyl)amino]-4-oxobutanoate

: 1334531-20-2
4-[(4-chloro-2-[(S)-hydroxy(2-methoxyphenyl)methyl]-6-methylphenyl)(2,2-dimethylpropyl)amino]-4-oxobutanoicacid

Guidance literature:: methyl 4-[(4-chloro-2-[(S)-hydroxy(2-methoxyphenyl)methyl]-6-methylphenyl)(2,2-dimethylpropyl)amino]-4-oxobutanoate; With water; potassium carbonate; In methanol; at 60 ℃; for 2.5h;

With citric acid; In water; ethyl acetate;
DOI:10.1016/j.bmc.2011.07.007

Reference yield:

: 1007652-06-3
N-[4-chloro-2-(trifluoromethyl)phenyl]-2,2-dimethylpropanamide

: 1334531-20-2
4-[(4-chloro-2-[(S)-hydroxy(2-methoxyphenyl)methyl]-6-methylphenyl)(2,2-dimethylpropyl)amino]-4-oxobutanoicacid

Guidance literature:: Multi-step reaction with 5 steps

1.1: sec.-butyllithium / tetrahydrofuran; hexane; cyclohexane / 0.5 h / -78 - 20 °C

1.2: 1.5 h / -78 - -50 °C

2.1: sodium bis(2-methoxyethoxy)aluminium dihydride / tetrahydrofuran; toluene / 4 h / 0 - 50 °C

2.2: 0.08 h

3.1: Chiralcel OD column / hexane; isopropyl alcohol / 20 °C / Resolution of racemate; HPLC conditions

4.1: sodium hydrogencarbonate / dichloromethane / 1 h / 20 °C / Cooling with ice

5.1: water; potassium carbonate / methanol / 2.5 h / 60 °C

With water; sec.-butyllithium; sodium hydrogencarbonate; potassium carbonate; sodium bis(2-methoxyethoxy)aluminium dihydride; In tetrahydrofuran; methanol; hexane; dichloromethane; cyclohexane; isopropyl alcohol; toluene;
DOI:10.1016/j.bmc.2011.07.007

Reference yield:

: 1334531-17-7
N-(4-chloro-2-[hydroxy(2-methoxyphenyl)methyl]-6-(trifluoromethyl)phenyl)-2,2-dimethylpropanamide

: 1334531-20-2
4-[(4-chloro-2-[(S)-hydroxy(2-methoxyphenyl)methyl]-6-methylphenyl)(2,2-dimethylpropyl)amino]-4-oxobutanoicacid

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium bis(2-methoxyethoxy)aluminium dihydride / tetrahydrofuran; toluene / 4 h / 0 - 50 °C

1.2: 0.08 h

2.1: Chiralcel OD column / hexane; isopropyl alcohol / 20 °C / Resolution of racemate; HPLC conditions

3.1: sodium hydrogencarbonate / dichloromethane / 1 h / 20 °C / Cooling with ice

4.1: water; potassium carbonate / methanol / 2.5 h / 60 °C

With water; sodium hydrogencarbonate; potassium carbonate; sodium bis(2-methoxyethoxy)aluminium dihydride; In tetrahydrofuran; methanol; hexane; dichloromethane; isopropyl alcohol; toluene;
DOI:10.1016/j.bmc.2011.07.007