N-(cyanomethyl)-N-methyl-5-[(4-methylbenzene)sulfonyl]-5H-[1,2,4]triazino[5,6-b]indole-3-carboxamide

Base Information

Chemical Name:N-(cyanomethyl)-N-methyl-5-[(4-methylbenzene)sulfonyl]-5H-[1,2,4]triazino[5,6-b]indole-3-carboxamide
CAS No.:1394236-92-0
Molecular Formula:C₂₀H₁₆N₆O₃S
Molecular Weight:420.451
Hs Code.:

Synonyms:N-(cyanomethyl)-N-methyl-5-[(4-methylbenzene)sulfonyl]-5H-[1,2,4]triazino[5,6-b]indole-3-carboxamide

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Chemical Property of N-(cyanomethyl)-N-methyl-5-[(4-methylbenzene)sulfonyl]-5H-[1,2,4]triazino[5,6-b]indole-3-carboxamide

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Technology Process of N-(cyanomethyl)-N-methyl-5-[(4-methylbenzene)sulfonyl]-5H-[1,2,4]triazino[5,6-b]indole-3-carboxamide

There total 3 articles about N-(cyanomethyl)-N-methyl-5-[(4-methylbenzene)sulfonyl]-5H-[1,2,4]triazino[5,6-b]indole-3-carboxamide 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: 95.0%

: 1394237-82-1
ethyl 5-[(4-methylbenzene)sulfonyl]-5H-[1,2,4]triazino[5,6-b]indole-3-carboxylate

: 25808-30-4
2-(methylamino)acetonitrile hydrochloride

: 1394236-92-0
N-(cyanomethyl)-N-methyl-5-[(4-methylbenzene)sulfonyl]-5H-[1,2,4]triazino[5,6-b]indole-3-carboxamide

Guidance literature:: With zirconium(IV) tert-butoxide; In dichloromethane; at 20 ℃; for 16h; Inert atmosphere;
DOI:10.3762/bjoc.8.93

Reference yield:

: 1394237-93-4
C₁₂H₁₀N₄O₂

: 1394236-92-0
N-(cyanomethyl)-N-methyl-5-[(4-methylbenzene)sulfonyl]-5H-[1,2,4]triazino[5,6-b]indole-3-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine / tetrahydrofuran / 0.5 h / 20 °C / Inert atmosphere

1.2: 7 h / 20 °C / Inert atmosphere

2.1: zirconium(IV) tert-butoxide / dichloromethane / 16 h / 20 °C / Inert atmosphere

With zirconium(IV) tert-butoxide; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.3762/bjoc.8.93

Reference yield:

: 91-56-5,1186480-61-4,84788-92-1
indole-2,3-dione

: 1394236-92-0
N-(cyanomethyl)-N-methyl-5-[(4-methylbenzene)sulfonyl]-5H-[1,2,4]triazino[5,6-b]indole-3-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: ethanol / 20 °C / Reflux; Inert atmosphere

1.2: 24 h / Inert atmosphere; Reflux

2.1: triethylamine / tetrahydrofuran / 0.5 h / 20 °C / Inert atmosphere

2.2: 7 h / 20 °C / Inert atmosphere

3.1: zirconium(IV) tert-butoxide / dichloromethane / 16 h / 20 °C / Inert atmosphere

With zirconium(IV) tert-butoxide; triethylamine; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.3762/bjoc.8.93