4-(4-nitrobenzyl)-2-<4-(pyridin-2-yl)thiazol-2-yl>pyridine N,N'-dioxide

Base Information

Chemical Name:4-(4-nitrobenzyl)-2-<4-(pyridin-2-yl)thiazol-2-yl>pyridine N,N'-dioxide
CAS No.:150223-68-0
Molecular Formula:C₂₀H₁₄N₄O₄S
Molecular Weight:406.422
Hs Code.:

Synonyms:4-(4-nitrobenzyl)-2-<4-(pyridin-2-yl)thiazol-2-yl>pyridine N,N'-dioxide

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Chemical Property of 4-(4-nitrobenzyl)-2-<4-(pyridin-2-yl)thiazol-2-yl>pyridine N,N'-dioxide

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Technology Process of 4-(4-nitrobenzyl)-2-<4-(pyridin-2-yl)thiazol-2-yl>pyridine N,N'-dioxide

There total 5 articles about 4-(4-nitrobenzyl)-2-<4-(pyridin-2-yl)thiazol-2-yl>pyridine N,N'-dioxide 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%

: 150223-67-9
4-(4-nitrobenzyl)-2-<4-(pyridin-2-yl)thiazol-2-yl>pyridine

: 150223-68-0
4-(4-nitrobenzyl)-2-<4-(pyridin-2-yl)thiazol-2-yl>pyridine N,N'-dioxide

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane;
DOI:10.1002/hlca.19960790129

Reference yield:

: 40086-66-6
2-Bromoacetylpyridine

: 150223-68-0
4-(4-nitrobenzyl)-2-<4-(pyridin-2-yl)thiazol-2-yl>pyridine N,N'-dioxide

Guidance literature:: Multi-step reaction with 2 steps

1: 61 percent / ethanol / 3 h / Heating

2: 82 percent / 3-chloroperbenzoic acid (50-55percent) / CH₂Cl₂

With 3-chloro-benzenecarboperoxoic acid; In ethanol; dichloromethane;
DOI:10.1002/hlca.19960790129

Reference yield:

: 1083-48-3
4-Nitrobenzylpyridin

: 150223-68-0
4-(4-nitrobenzyl)-2-<4-(pyridin-2-yl)thiazol-2-yl>pyridine N,N'-dioxide

Guidance literature:: Multi-step reaction with 5 steps

1: 83 percent / 3-chloroperbenzoic acid (50-55percent) / CH₂Cl₂ / 2 h

2: 53 percent / benzoyl chloride / CH₂Cl₂ / 0.5 h

3: 60 percent / NH₃ satd. in EtOH, H₂S / ethanol; CH₂Cl₂

4: 61 percent / ethanol / 3 h / Heating

5: 82 percent / 3-chloroperbenzoic acid (50-55percent) / CH₂Cl₂

With hydrogen sulfide; ammonia; benzoyl chloride; 3-chloro-benzenecarboperoxoic acid; In ethanol; dichloromethane;
DOI:10.1002/hlca.19960790129