methyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(pyridin-4-ylmethoxy)benzoylamino]propanoate

Base Information

Chemical Name:methyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(pyridin-4-ylmethoxy)benzoylamino]propanoate
CAS No.:1271521-78-8
Molecular Formula:C₂₂H₂₈N₄O₆S
Molecular Weight:476.554
Hs Code.:

Synonyms:methyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(pyridin-4-ylmethoxy)benzoylamino]propanoate

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Chemical Property of methyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(pyridin-4-ylmethoxy)benzoylamino]propanoate

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Technology Process of methyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(pyridin-4-ylmethoxy)benzoylamino]propanoate

There total 8 articles about methyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(pyridin-4-ylmethoxy)benzoylamino]propanoate 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: 62.0%

: 1271521-44-8
methyl (S)-3-(4-hydroxybenzoylamino)-2-(4-methanesulphonylpiperazin-1-yl)propanoate

: 1822-51-1
4-picolylchloride hydrochloride

: 1271521-78-8
methyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(pyridin-4-ylmethoxy)benzoylamino]propanoate

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 80 ℃; for 24h;

Reference yield:

: 99-76-3,156291-94-0
methyl 4-hydroxylbenzoate

: 1271521-78-8
methyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(pyridin-4-ylmethoxy)benzoylamino]propanoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide; tetrahydrofuran / 0.33 h / 20 °C

1.2: 24 h / 20 °C

2.1: sodium hydroxide; water / tetrahydrofuran; methanol / 18 h / 40 °C

2.2: pH 6

3.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 0.33 h

3.2: 19.5 h / 20 - 50 °C

4.1: sulfuric acid / tetrahydrofuran; methanol / 18 h / 20 °C

5.1: caesium carbonate / N,N-dimethyl-formamide / 24 h / 80 °C

With sulfuric acid; water; sodium hydride; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;

Reference yield:

: 906672-79-5
methyl 4-((2-methoxyethoxy)methoxy)benzoate

: 1271521-78-8
methyl (S)-2-(4-methanesulphonylpiperazin-1-yl)-3-[4-(pyridin-4-ylmethoxy)benzoylamino]propanoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydroxide; water / tetrahydrofuran; methanol / 18 h / 40 °C

1.2: pH 6

2.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 0.33 h

2.2: 19.5 h / 20 - 50 °C

3.1: sulfuric acid / tetrahydrofuran; methanol / 18 h / 20 °C

4.1: caesium carbonate / N,N-dimethyl-formamide / 24 h / 80 °C

With sulfuric acid; water; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;