(3R)-8-(3-trifluoromethylphenyl)-7-(naphthalen-1-ylsulfonamidomethyl)-5-oxo-2,3-dihydro-5-H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester

Base Information

Chemical Name:(3R)-8-(3-trifluoromethylphenyl)-7-(naphthalen-1-ylsulfonamidomethyl)-5-oxo-2,3-dihydro-5-H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester
CAS No.:1293894-82-2
Molecular Formula:C₂₇H₂₁F₃N₂O₅S₂
Molecular Weight:574.601
Hs Code.:

(3R)-8-(3-trifluoromethylphenyl)-7-(naphthalen-1-ylsulfonamidomethyl)-5-oxo-2,3-dihydro-5-H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester

Synonyms:(3R)-8-(3-trifluoromethylphenyl)-7-(naphthalen-1-ylsulfonamidomethyl)-5-oxo-2,3-dihydro-5-H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester

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Chemical Property of (3R)-8-(3-trifluoromethylphenyl)-7-(naphthalen-1-ylsulfonamidomethyl)-5-oxo-2,3-dihydro-5-H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester

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Technology Process of (3R)-8-(3-trifluoromethylphenyl)-7-(naphthalen-1-ylsulfonamidomethyl)-5-oxo-2,3-dihydro-5-H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester

There total 4 articles about (3R)-8-(3-trifluoromethylphenyl)-7-(naphthalen-1-ylsulfonamidomethyl)-5-oxo-2,3-dihydro-5-H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester 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: 81.0%

: 85-46-1
1-Naphthalenesulfonyl chloride

: 1293894-74-2
(3R)-8-(3-trifluoromethylphenyl)-7-aminomethyl-5-oxo-2,3-dihydro-5-H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester

: 1293894-82-2
(3R)-8-(3-trifluoromethylphenyl)-7-(naphthalen-1-ylsulfonamidomethyl)-5-oxo-2,3-dihydro-5-H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; Inert atmosphere;
DOI:10.1016/j.ejmech.2011.01.025

Reference yield:

: 864365-18-4
(4R)-2-(3-(trifluoromethyl)benzyl)-4,5-dihydrothiazole-4-carboxylic acid methyl ester

: 1293894-82-2
(3R)-8-(3-trifluoromethylphenyl)-7-(naphthalen-1-ylsulfonamidomethyl)-5-oxo-2,3-dihydro-5-H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: trifluoroacetic acid / 1,2-dichloro-ethane / 0.04 h / 120 °C / Microwave irradiation

2: sodium azide / N,N-dimethyl-formamide / 0.23 h / 20 °C / Inert atmosphere

3: ammonium chloride; zinc / ethanol; water / 0.33 h / 20 °C

4: triethylamine / dichloromethane / 20 °C / Inert atmosphere

With sodium azide; ammonium chloride; triethylamine; trifluoroacetic acid; zinc; In ethanol; dichloromethane; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2011.01.025

Reference yield:

: 1293894-72-0
(3R)-8-(3-trifluoromethylphenyl)-7-azidomethyl-5-oxo-2,3-dihydro-5-H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester

: 1293894-82-2
(3R)-8-(3-trifluoromethylphenyl)-7-(naphthalen-1-ylsulfonamidomethyl)-5-oxo-2,3-dihydro-5-H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: ammonium chloride; zinc / ethanol; water / 0.33 h / 20 °C

2: triethylamine / dichloromethane / 20 °C / Inert atmosphere

With ammonium chloride; triethylamine; zinc; In ethanol; dichloromethane; water;
DOI:10.1016/j.ejmech.2011.01.025