N-(2-(2-(5-bromopyridin-2-ylamino)-2-oxoethylthio)benzo[d]thiazol-6-yl)-2-methoxybenzamide

Base Information

Chemical Name:N-(2-(2-(5-bromopyridin-2-ylamino)-2-oxoethylthio)benzo[d]thiazol-6-yl)-2-methoxybenzamide
CAS No.:1316196-77-6
Molecular Formula:C₂₂H₁₇BrN₄O₃S₂
Molecular Weight:529.438
Hs Code.:

Synonyms:N-(2-(2-(5-bromopyridin-2-ylamino)-2-oxoethylthio)benzo[d]thiazol-6-yl)-2-methoxybenzamide

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Chemical Property of N-(2-(2-(5-bromopyridin-2-ylamino)-2-oxoethylthio)benzo[d]thiazol-6-yl)-2-methoxybenzamide

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Technology Process of N-(2-(2-(5-bromopyridin-2-ylamino)-2-oxoethylthio)benzo[d]thiazol-6-yl)-2-methoxybenzamide

There total 3 articles about N-(2-(2-(5-bromopyridin-2-ylamino)-2-oxoethylthio)benzo[d]thiazol-6-yl)-2-methoxybenzamide 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: 75.0%

: 1316196-17-4
C₁₄H₁₁BrN₄OS₂

: 21615-34-9
2-Methoxybenzoyl chloride

: 1316196-77-6
N-(2-(2-(5-bromopyridin-2-ylamino)-2-oxoethylthio)benzo[d]thiazol-6-yl)-2-methoxybenzamide

Guidance literature:: With triethylamine; In tetrahydrofuran;
DOI:10.3390/molecules17043933

Reference yield:

: 141454-61-7
2-chloro-N-(2-(5-bromo)pyridinyl)acetamide

: 1316196-77-6
N-(2-(2-(5-bromopyridin-2-ylamino)-2-oxoethylthio)benzo[d]thiazol-6-yl)-2-methoxybenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran / 5 h / 20 °C

2: triethylamine / tetrahydrofuran

With triethylamine; In tetrahydrofuran;
DOI:10.3390/molecules17043933

Reference yield:

: 1072-97-5
5-bromo-2-pyridylamine

: 1316196-77-6
N-(2-(2-(5-bromopyridin-2-ylamino)-2-oxoethylthio)benzo[d]thiazol-6-yl)-2-methoxybenzamide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / dichloromethane / 0 °C

2: triethylamine / tetrahydrofuran / 5 h / 20 °C

3: triethylamine / tetrahydrofuran

With potassium carbonate; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.3390/molecules17043933