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{2,5-Dimethyl-4-oxo-3-[2-(phenylsulfonyl)benzyl]-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl}acetic acid

Base Information
  • Chemical Name:{2,5-Dimethyl-4-oxo-3-[2-(phenylsulfonyl)benzyl]-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl}acetic acid
  • CAS No.:1415043-31-0
  • Molecular Formula:C24H24N2O5S
  • Molecular Weight:452.531
  • Hs Code.:
{2,5-Dimethyl-4-oxo-3-[2-(phenylsulfonyl)benzyl]-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl}acetic acid

Synonyms:{2,5-Dimethyl-4-oxo-3-[2-(phenylsulfonyl)benzyl]-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl}acetic acid

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Chemical Property of {2,5-Dimethyl-4-oxo-3-[2-(phenylsulfonyl)benzyl]-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl}acetic acid
Chemical Property:
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Technology Process of {2,5-Dimethyl-4-oxo-3-[2-(phenylsulfonyl)benzyl]-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl}acetic acid

There total 15 articles about {2,5-Dimethyl-4-oxo-3-[2-(phenylsulfonyl)benzyl]-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl}acetic 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:
Guidance literature:
Ethyl 2-(2,5-dimethyl-4-oxo-3-(2-(phenylsulfonyl)benzyl)-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-1-yl)acetate; With lithium hydroxide monohydrate; water; In tetrahydrofuran; at 20 ℃; for 1h;
With hydrogenchloride; In water; Product distribution / selectivity;
Guidance literature:
Multi-step reaction with 10 steps
1.1: potassium carbonate / dimethyl sulfoxide / 4 h / 100 °C
2.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 20 °C
3.1: toluene / 90 °C
4.1: hydrogen / palladium 10% on activated carbon / ethyl acetate / 3 h / 50 °C
5.1: dimethyl sulfoxide; trimethylsilyl bromide / acetonitrile / 2 h / 20 °C
6.1: ammonium acetate / ethanol / 15 h / 20 °C
7.1: sodium hydride / N,N-dimethyl-formamide / 0.25 h / 20 °C
8.1: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C
9.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.5 h / -78 °C
9.2: -78 - 20 °C
10.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 1 h / 20 °C
With lithium hydroxide monohydrate; trimethylsilyl bromide; ammonium acetate; water; hydrogen; sodium hydride; potassium carbonate; dimethyl sulfoxide; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid; lithium hexamethyldisilazane; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dichloromethane; dimethyl sulfoxide; ethyl acetate; N,N-dimethyl-formamide; toluene; acetonitrile;
Guidance literature:
Multi-step reaction with 10 steps
1.1: potassium carbonate / dimethyl sulfoxide / 4 h / 100 °C
2.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 20 °C
3.1: toluene / 90 °C
4.1: hydrogen / palladium 10% on activated carbon / ethyl acetate / 3 h / 50 °C
5.1: dimethyl sulfoxide; trimethylsilyl bromide / acetonitrile / 2 h / 20 °C
6.1: ammonium acetate / ethanol / 15 h / 20 °C
7.1: sodium hydride / N,N-dimethyl-formamide / 0.25 h / 20 °C
8.1: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C
9.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.5 h / -78 °C
9.2: -78 - 20 °C
10.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 1 h / 20 °C
With lithium hydroxide monohydrate; trimethylsilyl bromide; ammonium acetate; water; hydrogen; sodium hydride; potassium carbonate; dimethyl sulfoxide; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid; lithium hexamethyldisilazane; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dichloromethane; dimethyl sulfoxide; ethyl acetate; N,N-dimethyl-formamide; toluene; acetonitrile;
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