5-benzenesulfonyl-7,8-dimethoxy-2-phenylmethanesulfonyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

Base Information

Chemical Name:5-benzenesulfonyl-7,8-dimethoxy-2-phenylmethanesulfonyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole
CAS No.:267666-37-5
Molecular Formula:C₂₆H₂₆N₂O₆S₂
Molecular Weight:526.634
Hs Code.:

Synonyms:5-benzenesulfonyl-7,8-dimethoxy-2-phenylmethanesulfonyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

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Chemical Property of 5-benzenesulfonyl-7,8-dimethoxy-2-phenylmethanesulfonyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

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Technology Process of 5-benzenesulfonyl-7,8-dimethoxy-2-phenylmethanesulfonyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

There total 7 articles about 5-benzenesulfonyl-7,8-dimethoxy-2-phenylmethanesulfonyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole 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: 90.0%

: 267666-27-3
5-benzenesulfonyl-8-hydroxy-7-methoxy-2-phenylmethanesulfonyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

: 74-88-4
methyl iodide

: 267666-37-5
5-benzenesulfonyl-7,8-dimethoxy-2-phenylmethanesulfonyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

Guidance literature:: With potassium carbonate; In acetone; for 24h; Heating;
DOI:10.1021/jo9916176

Reference yield:

: 41979-39-9
4-piperidone hydrochloride

: 267666-37-5
5-benzenesulfonyl-7,8-dimethoxy-2-phenylmethanesulfonyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

Guidance literature:: Multi-step reaction with 5 steps

1: 95 percent / K₂CO₃ / H₂O; CHCl₃ / 20 °C

2: p-TsOH*H₂O / 10 h

3: 62 percent / AlCl₃; Et₃N / diethyl ether / 20 °C

4: 85 percent / TiCl₄; Ti(OiPr)4 / CH₂Cl₂ / -78 °C

5: 90 percent / K₂CO₃ / acetone / 24 h / Heating

With titanium(IV) isopropylate; aluminium trichloride; titanium tetrachloride; potassium carbonate; toluene-4-sulfonic acid; triethylamine; In diethyl ether; dichloromethane; chloroform; water; acetone; 1: Substitution / 2: Addition / 3: Elimination / 4: Elimination / 5: Methylation;
DOI:10.1021/jo9916176

Reference yield:

: 267666-14-8
4-methoxy-1-phenylmethanesulfonyl-1,2,3,6-tetrahydro-pyridine

: 267666-37-5
5-benzenesulfonyl-7,8-dimethoxy-2-phenylmethanesulfonyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / TiCl₄; Ti(OiPr)4 / CH₂Cl₂ / -78 °C

2: 90 percent / K₂CO₃ / acetone / 24 h / Heating

With titanium(IV) isopropylate; titanium tetrachloride; potassium carbonate; In dichloromethane; acetone; 1: Elimination / 2: Methylation;
DOI:10.1021/jo9916176