3-(4-Aminomethyl-benzenesulfonyl)-1-benzenesulfonyl-1H-indole-4-carboxylic acid methyl ester

Base Information

Chemical Name:3-(4-Aminomethyl-benzenesulfonyl)-1-benzenesulfonyl-1H-indole-4-carboxylic acid methyl ester
CAS No.:1025830-33-4
Molecular Formula:C₂₃H₂₀N₂O₆S₂
Molecular Weight:484.554
Hs Code.:

Synonyms:3-(4-Aminomethyl-benzenesulfonyl)-1-benzenesulfonyl-1H-indole-4-carboxylic acid methyl ester

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Chemical Property of 3-(4-Aminomethyl-benzenesulfonyl)-1-benzenesulfonyl-1H-indole-4-carboxylic acid methyl ester

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Technology Process of 3-(4-Aminomethyl-benzenesulfonyl)-1-benzenesulfonyl-1H-indole-4-carboxylic acid methyl ester

There total 6 articles about 3-(4-Aminomethyl-benzenesulfonyl)-1-benzenesulfonyl-1H-indole-4-carboxylic 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:

: 39830-66-5
methyl 1H-indole-4-carboxylate

: 1025830-33-4
3-(4-Aminomethyl-benzenesulfonyl)-1-benzenesulfonyl-1H-indole-4-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) Et₃N, SO₂Cl₂ / 1.) CH₂Cl₂, -20 deg C, 1 h, 2.) CH₂Cl₂, RT, 17 h

2: KOH / 1,2-dimethoxy-ethane / 1 h

3: 30percent aq. H₂O₂, glacial acetic acid / 0.5 h / Heating

4: NBS, benzoyl peroxide / CCl₄ / a) reflux, 3 h, b) RT, 17 h

5: dimethylformamide / 2 h / 50 °C

6: TFA / 0.75 h / Ambient temperature

With potassium hydroxide; N-Bromosuccinimide; sulfuryl dichloride; Perbenzoic acid; dihydrogen peroxide; acetic acid; triethylamine; trifluoroacetic acid; In tetrachloromethane; 1,2-dimethoxyethane; N,N-dimethyl-formamide;
DOI:10.1021/jm970389+

Reference yield:

: 103-19-5
di(p-tolyl) disulfide

: 1025830-33-4
3-(4-Aminomethyl-benzenesulfonyl)-1-benzenesulfonyl-1H-indole-4-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) Et₃N, SO₂Cl₂ / 1.) CH₂Cl₂, -20 deg C, 1 h, 2.) CH₂Cl₂, RT, 17 h

2: KOH / 1,2-dimethoxy-ethane / 1 h

3: 30percent aq. H₂O₂, glacial acetic acid / 0.5 h / Heating

4: NBS, benzoyl peroxide / CCl₄ / a) reflux, 3 h, b) RT, 17 h

5: dimethylformamide / 2 h / 50 °C

6: TFA / 0.75 h / Ambient temperature

With potassium hydroxide; N-Bromosuccinimide; sulfuryl dichloride; Perbenzoic acid; dihydrogen peroxide; acetic acid; triethylamine; trifluoroacetic acid; In tetrachloromethane; 1,2-dimethoxyethane; N,N-dimethyl-formamide;
DOI:10.1021/jm970389+

Reference yield:

: 175675-85-1
3-p-Tolylsulfanyl-1H-indole-4-carboxylic acid methyl ester

: 1025830-33-4
3-(4-Aminomethyl-benzenesulfonyl)-1-benzenesulfonyl-1H-indole-4-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: KOH / 1,2-dimethoxy-ethane / 1 h

2: 30percent aq. H₂O₂, glacial acetic acid / 0.5 h / Heating

3: NBS, benzoyl peroxide / CCl₄ / a) reflux, 3 h, b) RT, 17 h

4: dimethylformamide / 2 h / 50 °C

5: TFA / 0.75 h / Ambient temperature

With potassium hydroxide; N-Bromosuccinimide; Perbenzoic acid; dihydrogen peroxide; acetic acid; trifluoroacetic acid; In tetrachloromethane; 1,2-dimethoxyethane; N,N-dimethyl-formamide;
DOI:10.1021/jm970389+