2-[1-benzenesulfonyl-3-(furan-2-ylcarbamoylmethyl)-1H-indol-2-yl]acrylic acid methyl ester

Base Information

Chemical Name:2-[1-benzenesulfonyl-3-(furan-2-ylcarbamoylmethyl)-1H-indol-2-yl]acrylic acid methyl ester
CAS No.:849738-60-9
Molecular Formula:C₂₄H₂₀N₂O₆S
Molecular Weight:464.499
Hs Code.:

Synonyms:2-[1-benzenesulfonyl-3-(furan-2-ylcarbamoylmethyl)-1H-indol-2-yl]acrylic acid methyl ester

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Chemical Property of 2-[1-benzenesulfonyl-3-(furan-2-ylcarbamoylmethyl)-1H-indol-2-yl]acrylic acid methyl ester

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Technology Process of 2-[1-benzenesulfonyl-3-(furan-2-ylcarbamoylmethyl)-1H-indol-2-yl]acrylic acid methyl ester

There total 7 articles about 2-[1-benzenesulfonyl-3-(furan-2-ylcarbamoylmethyl)-1H-indol-2-yl]acrylic acid methyl ester 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:

: 56267-47-1
tert-butyl furan-2-ylcarbamate

: 2-(1-benzenesulfonyl-3-chlorocarbonylmethyl-1H-indol-2-yl)-acrylic acid methyl ester

: 849738-60-9
2-[1-benzenesulfonyl-3-(furan-2-ylcarbamoylmethyl)-1H-indol-2-yl]acrylic acid methyl ester

Guidance literature:: tert-butyl furan-2-ylcarbamate; 2-(1-benzenesulfonyl-3-chlorocarbonylmethyl-1H-indol-2-yl)-acrylic acid methyl ester; With n-butyllithium; In tetrahydrofuran; hexane; at 0 ℃; for 0.333333h;

With magnesium(II) perchlorate; In acetonitrile; at 50 ℃; for 1h;
DOI:10.1021/jo047834a

Reference yield:

: 140920-82-7
1-(O-tert-butyldimethylsilyl)-2-<3-(1-phenylsulfonyl)indolyl>ethanol

: 849738-60-9
2-[1-benzenesulfonyl-3-(furan-2-ylcarbamoylmethyl)-1H-indol-2-yl]acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: n-BuLi / tetrahydrofuran; hexane / -78 - 20 °C

1.2: 63 percent / tetrahydrofuran; hexane / 0.5 h / -78 °C

2.1: BF₃*OEt₂ / CH₂Cl₂ / 2 h / 20 °C

3.1: Et₃N; DMAP / CH₂Cl₂ / 0.17 h / 0 °C

4.1: p-TsOH*H₂O / benzene / 1 h / Heating

5.1: 1.4 g / Na₂CO₃ / methanol; H₂O / 0.5 h / Heating

6.1: Jones' reagent / acetone / 2 h / 20 °C

6.2: oxalyl chloride; DMF / CH₂Cl₂ / 1 h / 25 °C

7.1: n-BuLi / tetrahydrofuran; hexane / 0.33 h / 0 °C

7.2: 0.053 g / Mg(ClO₄)2 / acetonitrile / 1 h / 50 °C

With dmap; n-butyllithium; jones' reagent; boron trifluoride diethyl etherate; sodium carbonate; toluene-4-sulfonic acid; triethylamine; In tetrahydrofuran; methanol; hexane; dichloromethane; water; acetone; benzene; 6.1: Jones' oxidation;
DOI:10.1021/jo047834a

Reference yield:

: 849738-67-6
2-[1-benzenesulfonyl-3-(2-hydroxyethyl)-1H-indol-2-yl]acrylic acid methyl ester

: 849738-60-9
2-[1-benzenesulfonyl-3-(furan-2-ylcarbamoylmethyl)-1H-indol-2-yl]acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: Jones' reagent / acetone / 2 h / 20 °C

1.2: oxalyl chloride; DMF / CH₂Cl₂ / 1 h / 25 °C

2.1: n-BuLi / tetrahydrofuran; hexane / 0.33 h / 0 °C

2.2: 0.053 g / Mg(ClO₄)2 / acetonitrile / 1 h / 50 °C

With n-butyllithium; jones' reagent; In tetrahydrofuran; hexane; acetone; 1.1: Jones' oxidation;
DOI:10.1021/jo047834a