N-(4-bromo-2-(trifluoromethoxy)benzyl)-2-(2,2-difluoroethyl)-3-oxo-2,3-dihydro-[1,2,4]triazolo[4,3-a]pyridine-6-carboxamide

Base Information

• Chemical Name: N-(4-bromo-2-(trifluoromethoxy)benzyl)-2-(2,2-difluoroethyl)-3-oxo-2,3-dihydro-[1,2,4]triazolo[4,3-a]pyridine-6-carboxamide
• CAS No.: 1241826-85-6
• Molecular Formula: C₁₇H₁₂BrF₅N₄O₃
• Molecular Weight: 495.203

Synonyms:N-(4-bromo-2-(trifluoromethoxy)benzyl)-2-(2,2-difluoroethyl)-3-oxo-2,3-dihydro-[1,2,4]triazolo[4,3-a]pyridine-6-carboxamide

Chemical Property of N-(4-bromo-2-(trifluoromethoxy)benzyl)-2-(2,2-difluoroethyl)-3-oxo-2,3-dihydro-[1,2,4]triazolo[4,3-a]pyridine-6-carboxamide

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Technology Process of N-(4-bromo-2-(trifluoromethoxy)benzyl)-2-(2,2-difluoroethyl)-3-oxo-2,3-dihydro-[1,2,4]triazolo[4,3-a]pyridine-6-carboxamide

There total 4 articles about N-(4-bromo-2-(trifluoromethoxy)benzyl)-2-(2,2-difluoroethyl)-3-oxo-2,3-dihydro-[1,2,4]triazolo[4,3-a]pyridine-6-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:

1,1-difluoro-2-iodoethane (598-39-0) → N-(4-bromo-2-(trifluoromethoxy)benzyl)-2-(2,2-difluoroethyl)-3-oxo-2,3-dihydro-[1,2,4]triazolo[4,3-a]pyridine-6-carboxamide (1241826-85-6)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 65 ℃; for 16h;

Reference yield:

1,1-difluoro-2-iodoethane (598-39-0) + (R)-5-chloro-6-(pyrrolidin-3-yloxy)pyridine-3-sulfonamide + 2',3'-dihydro-1'H-spiro[cyclopropane-1,4'-isoquinolin]-7'-amine trifluoroacetate (1395030-57-5) → N-(4-bromo-2-(trifluoromethoxy)benzyl)-2-(2,2-difluoroethyl)-3-oxo-2,3-dihydro-[1,2,4]triazolo[4,3-a]pyridine-6-carboxamide (1241826-85-6) + (R)-5-chloro-6-(1-(2,2-difluoroethyl)pyrrolidin-3-yloxy)pyridine-3-sulfonamide

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 65 ℃; for 16h;

Reference yield:

1,1-difluoro-2-iodoethane (598-39-0) + (R)-5-chloro-6-(pyrrolidin-3-yloxy)pyridine-3-sulfonamide + 2',3'-dihydro-1'H-spiro[cyclopropane-1,4'-isoquinolin]-7'-amine trifluoroacetate (1395030-57-5) + C13H9F3N4S (1254165-70-2) + 1H-pyrrolo[3,2-b]pyridine-6-chloro-5-carboxylic acid ethyl ester (872355-69-6) + 1,1-difluoro-2-iodoethane (598-39-0) → N-(4-bromo-2-(trifluoromethoxy)benzyl)-2-(2,2-difluoroethyl)-3-oxo-2,3-dihydro-[1,2,4]triazolo[4,3-a]pyridine-6-carboxamide (1241826-85-6) + (R)-5-chloro-6-(1-(2,2-difluoroethyl)pyrrolidin-3-yloxy)pyridine-3-sulfonamide + methyl 1-(2,2-difluoroethyl)-1H-indole-5-carboxylate (1252782-51-6) + C15H11F5N4S (1254165-78-0) + 2'-(2,2-difluoroethyl)-2',3'-dihydro-1'H-spiro[cyclopropane-1,4'-isoquinolin]-7'-amine (1395030-58-6)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 65 ℃; for 16h;

upstream raw materials:

1,1-difluoro-2-iodoethane

2',3'-dihydro-1'H-spiro[cyclopropane-1,4'-isoquinolin]-7'-amine trifluoroacetate

C₁₃H₉F₃N₄S

1H-pyrrolo[3,2-b]pyridine-6-chloro-5-carboxylic acid ethyl ester

Downstream raw materials:

N-(4-cyano-2-(trifluoromethoxy)benzyl)-2-(2,2-difluoroethyl)-3-oxo-2,3-dihydro-[1,2,4]triazolo[4,3-a]pyridine-6-carboxamide

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