tert-butyl (8-(4-benzyloxy)-2-oxopyridin-1(2H)-yl)-3,4,5,6-tetrahydroazepino[4,3-b]indole-2(1H)-carboxylate

Base Information

Chemical Name:tert-butyl (8-(4-benzyloxy)-2-oxopyridin-1(2H)-yl)-3,4,5,6-tetrahydroazepino[4,3-b]indole-2(1H)-carboxylate
CAS No.:1260494-19-6
Molecular Formula:C₂₉H₃₁N₃O₄
Molecular Weight:485.583
Hs Code.:

Synonyms:tert-butyl (8-(4-benzyloxy)-2-oxopyridin-1(2H)-yl)-3,4,5,6-tetrahydroazepino[4,3-b]indole-2(1H)-carboxylate

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Chemical Property of tert-butyl (8-(4-benzyloxy)-2-oxopyridin-1(2H)-yl)-3,4,5,6-tetrahydroazepino[4,3-b]indole-2(1H)-carboxylate

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Technology Process of tert-butyl (8-(4-benzyloxy)-2-oxopyridin-1(2H)-yl)-3,4,5,6-tetrahydroazepino[4,3-b]indole-2(1H)-carboxylate

There total 5 articles about tert-butyl (8-(4-benzyloxy)-2-oxopyridin-1(2H)-yl)-3,4,5,6-tetrahydroazepino[4,3-b]indole-2(1H)-carboxylate 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: 55.0%

: 1260494-18-5
tert-butyl (8-(4-benzyloxy)-2-oxopyridin-1(2H)-yl)-6-tosyl-3,4,5,6-tetrahydroazepino[4,3-b]indole-2(1H)-carboxylate

: 1260494-19-6
tert-butyl (8-(4-benzyloxy)-2-oxopyridin-1(2H)-yl)-3,4,5,6-tetrahydroazepino[4,3-b]indole-2(1H)-carboxylate

Guidance literature:: With sodium hydroxide; In methanol; dichloromethane; for 18h; Reflux;

Reference yield:

: 1260494-15-2
8-bromo-2,3,4,5-tetrahydroazepino[4,3-b]indol-1(6H)-one

: 1260494-19-6
tert-butyl (8-(4-benzyloxy)-2-oxopyridin-1(2H)-yl)-3,4,5,6-tetrahydroazepino[4,3-b]indole-2(1H)-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: borane-THF / tetrahydrofuran / 48 h / Reflux

1.2: 2 h / Reflux

1.3: 18 h / 20 °C

2.1: tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide / toluene; water / 18 h

3.1: caesium carbonate; 8-quinolinol / copper(l) iodide / dimethyl sulfoxide / 18 h / 130 °C / Inert atmosphere

4.1: sodium hydroxide / dichloromethane; methanol / 18 h / Reflux

With 8-quinolinol; borane-THF; tetra(n-butyl)ammonium hydrogensulfate; caesium carbonate; sodium hydroxide; copper(l) iodide; In tetrahydrofuran; methanol; dichloromethane; water; dimethyl sulfoxide; toluene;

Reference yield:

: 1260494-14-1
7-bromo-2,3-dihydro-1H-carbazol-4(9H)-one oxime

: 1260494-19-6
tert-butyl (8-(4-benzyloxy)-2-oxopyridin-1(2H)-yl)-3,4,5,6-tetrahydroazepino[4,3-b]indole-2(1H)-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: diphenyl phosphoryl azide / 4.5 h / 100 °C

2.1: borane-THF / tetrahydrofuran / 48 h / Reflux

2.2: 2 h / Reflux

2.3: 18 h / 20 °C

3.1: tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide / toluene; water / 18 h

4.1: caesium carbonate; 8-quinolinol / copper(l) iodide / dimethyl sulfoxide / 18 h / 130 °C / Inert atmosphere

5.1: sodium hydroxide / dichloromethane; methanol / 18 h / Reflux

With 8-quinolinol; borane-THF; diphenyl phosphoryl azide; tetra(n-butyl)ammonium hydrogensulfate; caesium carbonate; sodium hydroxide; copper(l) iodide; In tetrahydrofuran; methanol; dichloromethane; water; dimethyl sulfoxide; toluene;