(S)-3-{4-[4-(3-aminopropoxy)-2,6-dichlorobenzoylamino]phenyl}-2-[2-chloro-4-(3-hydroxybenzylcarbamoyl)benzoylamino]propionic acid

Base Information

Chemical Name:(S)-3-{4-[4-(3-aminopropoxy)-2,6-dichlorobenzoylamino]phenyl}-2-[2-chloro-4-(3-hydroxybenzylcarbamoyl)benzoylamino]propionic acid
CAS No.:1449061-33-9
Molecular Formula:C₃₄H₃₁Cl₃N₄O₇
Molecular Weight:714.002
Hs Code.:

Synonyms:(S)-3-{4-[4-(3-aminopropoxy)-2,6-dichlorobenzoylamino]phenyl}-2-[2-chloro-4-(3-hydroxybenzylcarbamoyl)benzoylamino]propionic acid

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Chemical Property of (S)-3-{4-[4-(3-aminopropoxy)-2,6-dichlorobenzoylamino]phenyl}-2-[2-chloro-4-(3-hydroxybenzylcarbamoyl)benzoylamino]propionic acid

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Technology Process of (S)-3-{4-[4-(3-aminopropoxy)-2,6-dichlorobenzoylamino]phenyl}-2-[2-chloro-4-(3-hydroxybenzylcarbamoyl)benzoylamino]propionic acid

There total 9 articles about (S)-3-{4-[4-(3-aminopropoxy)-2,6-dichlorobenzoylamino]phenyl}-2-[2-chloro-4-(3-hydroxybenzylcarbamoyl)benzoylamino]propionic acid 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:

: (S)-3-{4-[4-(3-aminopropoxy)-2,6-dichlorobenzoylamino]phenyl}[2-chloro-4-(3-hydroxybenzylcarbamoyl)benzoylamino]propionic acid methyl ester hydrochloride

: 1449061-33-9
(S)-3-{4-[4-(3-aminopropoxy)-2,6-dichlorobenzoylamino]phenyl}-2-[2-chloro-4-(3-hydroxybenzylcarbamoyl)benzoylamino]propionic acid

Guidance literature:: With water; sodium hydroxide; In methanol; at 20 ℃;

Reference yield:

: 1449061-30-6
(S)-2-{4-[3-(tert-butyldimethylsilanyloxy)benzylcarbamoyl]-2-chlorobenzoylamino}-3-[4-(2,6-dichloro-4-hydroxybenzoylamino)phenyl]propionic acid methyl ester

: 1449061-33-9
(S)-3-{4-[4-(3-aminopropoxy)-2,6-dichlorobenzoylamino]phenyl}-2-[2-chloro-4-(3-hydroxybenzylcarbamoyl)benzoylamino]propionic acid

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / N,N-dimethyl-formamide; acetone / 75 °C

2: methanol; chloro-trimethyl-silane / 20 °C

3: water; sodium hydroxide / methanol / 20 °C

With methanol; chloro-trimethyl-silane; water; potassium carbonate; sodium hydroxide; In methanol; N,N-dimethyl-formamide; acetone;

Reference yield:

: 1449061-25-9
(S)-2-tert-butoxycarbonylamino-3-[4-(2,6-dichloro-4-triisopropylsilanyloxybenzoylamino)phenyl]propionic acid methyl ester

: 1449061-33-9
(S)-3-{4-[4-(3-aminopropoxy)-2,6-dichlorobenzoylamino]phenyl}-2-[2-chloro-4-(3-hydroxybenzylcarbamoyl)benzoylamino]propionic acid

Guidance literature:: Multi-step reaction with 6 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 °C

2: methanol; chloro-trimethyl-silane / 20 °C

3: N-ethyl-N,N-diisopropylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / N,N-dimethyl-formamide / 20 °C

4: potassium carbonate / N,N-dimethyl-formamide; acetone / 75 °C

5: methanol; chloro-trimethyl-silane / 20 °C

6: water; sodium hydroxide / methanol / 20 °C

With methanol; chloro-trimethyl-silane; tetrabutyl ammonium fluoride; water; potassium carbonate; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetone;