(3R)-6-bromo-8-[1-(4-methyl-benzyl)-1H-[1,2,3]triazol-4-yl]-7-naphthalen-1-ylmethyl-5-oxo-2,3-dihydro-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid

Base Information

Chemical Name:(3R)-6-bromo-8-[1-(4-methyl-benzyl)-1H-[1,2,3]triazol-4-yl]-7-naphthalen-1-ylmethyl-5-oxo-2,3-dihydro-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid
CAS No.:1394135-70-6
Molecular Formula:C₂₉H₂₃BrN₄O₃S
Molecular Weight:587.497
Hs Code.:

Synonyms:(3R)-6-bromo-8-[1-(4-methyl-benzyl)-1H-[1,2,3]triazol-4-yl]-7-naphthalen-1-ylmethyl-5-oxo-2,3-dihydro-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid

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Chemical Property of (3R)-6-bromo-8-[1-(4-methyl-benzyl)-1H-[1,2,3]triazol-4-yl]-7-naphthalen-1-ylmethyl-5-oxo-2,3-dihydro-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid

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Technology Process of (3R)-6-bromo-8-[1-(4-methyl-benzyl)-1H-[1,2,3]triazol-4-yl]-7-naphthalen-1-ylmethyl-5-oxo-2,3-dihydro-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid

There total 5 articles about (3R)-6-bromo-8-[1-(4-methyl-benzyl)-1H-[1,2,3]triazol-4-yl]-7-naphthalen-1-ylmethyl-5-oxo-2,3-dihydro-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid 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: 82.0%

: 1394135-57-9
(3R)-6-bromo-8-[1-(4-methyl-benzyl)-1H-[1,2,3]triazol-4-yl]-7-naphthalen-1-ylmethyl-5-oxo-2,3-dihydro-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester

: 1394135-70-6
(3R)-6-bromo-8-[1-(4-methyl-benzyl)-1H-[1,2,3]triazol-4-yl]-7-naphthalen-1-ylmethyl-5-oxo-2,3-dihydro-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid

Guidance literature:: (3R)-6-bromo-8-[1-(4-methyl-benzyl)-1H-[1,2,3]triazol-4-yl]-7-naphthalen-1-ylmethyl-5-oxo-2,3-dihydro-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester; With lithium hydroxide; In tetrahydrofuran; water; at 20 ℃; for 17h;

With hydrogenchloride; In tetrahydrofuran; water; ethyl acetate; pH=1;
DOI:10.1016/j.ejmech.2012.06.018

Reference yield:

: C₂₅H₂₄BrNO₃SSi

: 1394135-70-6
(3R)-6-bromo-8-[1-(4-methyl-benzyl)-1H-[1,2,3]triazol-4-yl]-7-naphthalen-1-ylmethyl-5-oxo-2,3-dihydro-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: methanol; potassium carbonate / tetrahydrofuran / 0.25 h / 20 °C

2.1: sodium azide; copper(II) sulfate; sodium L-ascorbate / water; N,N-dimethyl-formamide / 16 h / 70 °C

3.1: lithium hydroxide / tetrahydrofuran; water / 17 h / 20 °C

3.2: pH 1

With methanol; sodium azide; potassium carbonate; copper(II) sulfate; sodium L-ascorbate; lithium hydroxide; In tetrahydrofuran; water; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2012.06.018

Reference yield:

: 1394135-49-9
(3R)-6-bromo-7-naphthalen-1-ylmethyl-5-oxo-8-ethynyl-2,3-dihydro-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester

: 1394135-70-6
(3R)-6-bromo-8-[1-(4-methyl-benzyl)-1H-[1,2,3]triazol-4-yl]-7-naphthalen-1-ylmethyl-5-oxo-2,3-dihydro-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium azide; copper(II) sulfate; sodium L-ascorbate / water; N,N-dimethyl-formamide / 16 h / 70 °C

2.1: lithium hydroxide / tetrahydrofuran; water / 17 h / 20 °C

2.2: pH 1

With sodium azide; copper(II) sulfate; sodium L-ascorbate; lithium hydroxide; In tetrahydrofuran; water; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2012.06.018