5-(4-(benzyloxy)phenyl)-6-(methylsulfonyl)-2-tosyl-1,2,3,4,5,6-hexahydroazepino[4,3-b]indole

Base Information

Chemical Name:5-(4-(benzyloxy)phenyl)-6-(methylsulfonyl)-2-tosyl-1,2,3,4,5,6-hexahydroazepino[4,3-b]indole
CAS No.:1602922-72-4
Molecular Formula:C₃₃H₃₂N₂O₅S₂
Molecular Weight:600.759
Hs Code.:

Synonyms:5-(4-(benzyloxy)phenyl)-6-(methylsulfonyl)-2-tosyl-1,2,3,4,5,6-hexahydroazepino[4,3-b]indole

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Chemical Property of 5-(4-(benzyloxy)phenyl)-6-(methylsulfonyl)-2-tosyl-1,2,3,4,5,6-hexahydroazepino[4,3-b]indole

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Technology Process of 5-(4-(benzyloxy)phenyl)-6-(methylsulfonyl)-2-tosyl-1,2,3,4,5,6-hexahydroazepino[4,3-b]indole

There total 4 articles about 5-(4-(benzyloxy)phenyl)-6-(methylsulfonyl)-2-tosyl-1,2,3,4,5,6-hexahydroazepino[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: 76.0%

: C₃₃H₃₄N₂O₆S₂

: 1602922-72-4
5-(4-(benzyloxy)phenyl)-6-(methylsulfonyl)-2-tosyl-1,2,3,4,5,6-hexahydroazepino[4,3-b]indole

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 0 ℃;
DOI:10.1021/jo500308y

Reference yield:

: 161040-05-7
N-(but-3-yn-1-yl)-4-methylbenzenesulfonamide

: 1602922-72-4
5-(4-(benzyloxy)phenyl)-6-(methylsulfonyl)-2-tosyl-1,2,3,4,5,6-hexahydroazepino[4,3-b]indole

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / 0 °C

1.2: 60 °C

2.1: n-butyllithium / tetrahydrofuran / 0.5 h / -78 °C

2.2: 0.5 h / -78 °C

3.1: silver(I) acetate / acetonitrile / 0.33 h / 20 °C

4.1: trifluoroacetic acid / dichloromethane / 0 °C

With n-butyllithium; silver(I) acetate; sodium hydride; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; acetonitrile; mineral oil;
DOI:10.1021/jo500308y

Reference yield:

: 1602922-92-8
N-(5-hydroxy-5-(2-(methylsulfonamido)phenyl)pent-3-yn-1-yl)-N-(4-benzyloxybenzyl)-4-methylbenzenesulfonamide

: 1602922-72-4
5-(4-(benzyloxy)phenyl)-6-(methylsulfonyl)-2-tosyl-1,2,3,4,5,6-hexahydroazepino[4,3-b]indole

Guidance literature:: Multi-step reaction with 2 steps

1: silver(I) acetate / acetonitrile / 0.33 h / 20 °C

2: trifluoroacetic acid / dichloromethane / 0 °C

With silver(I) acetate; trifluoroacetic acid; In dichloromethane; acetonitrile;
DOI:10.1021/jo500308y