5-((4-chloro-N-((tetrahydro-2H-pyran-4-yl)methyl)phenylsulfonamido)-methyl)-2-methoxybenzoic acid

Base Information

Chemical Name:5-((4-chloro-N-((tetrahydro-2H-pyran-4-yl)methyl)phenylsulfonamido)-methyl)-2-methoxybenzoic acid
CAS No.:1429647-00-6
Molecular Formula:C₂₀H₂₂ClNO₅S
Molecular Weight:423.917
Hs Code.:

Synonyms:5-((4-chloro-N-((tetrahydro-2H-pyran-4-yl)methyl)phenylsulfonamido)-methyl)-2-methoxybenzoic acid

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Chemical Property of 5-((4-chloro-N-((tetrahydro-2H-pyran-4-yl)methyl)phenylsulfonamido)-methyl)-2-methoxybenzoic acid

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Technology Process of 5-((4-chloro-N-((tetrahydro-2H-pyran-4-yl)methyl)phenylsulfonamido)-methyl)-2-methoxybenzoic acid

There total 3 articles about 5-((4-chloro-N-((tetrahydro-2H-pyran-4-yl)methyl)phenylsulfonamido)-methyl)-2-methoxybenzoic 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: 98.0%

: 1429646-99-0
methyl 5-((4-chloro-N-((tetrahydro-2H-pyran-4-yl)methyl)phenylsulfonamido)-methyl)-2-methoxybenzoate

: 1429647-00-6
5-((4-chloro-N-((tetrahydro-2H-pyran-4-yl)methyl)phenylsulfonamido)-methyl)-2-methoxybenzoic acid

Guidance literature:: methyl 5-((4-chloro-N-((tetrahydro-2H-pyran-4-yl)methyl)phenylsulfonamido)-methyl)-2-methoxybenzoate; With lithium hydroxide monohydrate; In tetrahydrofuran; water; at 55 ℃; for 6h;

With hydrogenchloride; In tetrahydrofuran; water; at 20 ℃; pH=2;

Reference yield:

: 98-60-2
4-chlorobenzenesulfonyl chloride

: 1429647-00-6
5-((4-chloro-N-((tetrahydro-2H-pyran-4-yl)methyl)phenylsulfonamido)-methyl)-2-methoxybenzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / tetrahydrofuran / 16 h / 20 °C

2.1: caesium carbonate / N,N-dimethyl-formamide / 3 h / 20 °C

3.1: lithium hydroxide monohydrate / tetrahydrofuran; water / 6 h / 55 °C

3.2: 20 °C / pH 2

With lithium hydroxide monohydrate; potassium carbonate; caesium carbonate; In tetrahydrofuran; water; N,N-dimethyl-formamide;

Reference yield:

: 2417-72-3
Methyl 4-(bromomethyl)benzoate

: 1429647-68-6
4-chloro-N-((tetrahydro-2H-pyran-4-yl)methyl)benzenesulfonamide

: 1429647-00-6
5-((4-chloro-N-((tetrahydro-2H-pyran-4-yl)methyl)phenylsulfonamido)-methyl)-2-methoxybenzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: caesium carbonate / N,N-dimethyl-formamide / 3 h / 20 °C

2.1: lithium hydroxide monohydrate / tetrahydrofuran; water / 6 h / 55 °C

2.2: 20 °C / pH 2

With lithium hydroxide monohydrate; caesium carbonate; In tetrahydrofuran; water; N,N-dimethyl-formamide;