4-nitrophenyl N-[(5-[[3-(trifluoromethyl)benzene]sulfonyl]pyridin-2-yl)methyl]carbamate

Base Information

• Chemical Name: 4-nitrophenyl N-[(5-[[3-(trifluoromethyl)benzene]sulfonyl]pyridin-2-yl)methyl]carbamate
• CAS No.: 1454252-76-6
• Molecular Formula: C₂₀H₁₄F₃N₃O₆S
• Molecular Weight: 481.409
• Mol file: 1454252-76-6.mol

Synonyms:4-nitrophenyl N-[(5-[[3-(trifluoromethyl)benzene]sulfonyl]pyridin-2-yl)methyl]carbamate

Chemical Property of 4-nitrophenyl N-[(5-[[3-(trifluoromethyl)benzene]sulfonyl]pyridin-2-yl)methyl]carbamate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-nitrophenyl N-[(5-[[3-(trifluoromethyl)benzene]sulfonyl]pyridin-2-yl)methyl]carbamate

There total 5 articles about 4-nitrophenyl N-[(5-[[3-(trifluoromethyl)benzene]sulfonyl]pyridin-2-yl)methyl]carbamate 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: 26.0%

(5-[[3-(trifluoromethyl)benzene]sulfonyl]pyridin-2-yl)methanamine (1374864-85-3) + 4-Nitrophenyl chloroformate (7693-46-1) → 4-nitrophenyl N-[(5-[[3-(trifluoromethyl)benzene]sulfonyl]pyridin-2-yl)methyl]carbamate (1454252-76-6)

Guidance literature:

In toluene; for 3h; Reflux;

Reference yield:

2-Cyano-5-bromopyridine (97483-77-7) → 4-nitrophenyl N-[(5-[[3-(trifluoromethyl)benzene]sulfonyl]pyridin-2-yl)methyl]carbamate (1454252-76-6)

Guidance literature:

Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl-formamide / 120 °C

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 2 h / 0 - 20 °C

3: hydrazine hydrate / methanol / 0.17 h / 0 - 20 °C

4: toluene / 3 h / Reflux

With potassium carbonate; hydrazine hydrate; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane; N,N-dimethyl-formamide; toluene;

Reference yield:

3-trifluoromethyl-thiophenol (937-00-8) → 4-nitrophenyl N-[(5-[[3-(trifluoromethyl)benzene]sulfonyl]pyridin-2-yl)methyl]carbamate (1454252-76-6)

Guidance literature:

Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl-formamide / 120 °C

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 2 h / 0 - 20 °C

3: hydrazine hydrate / methanol / 0.17 h / 0 - 20 °C

4: toluene / 3 h / Reflux

With potassium carbonate; hydrazine hydrate; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane; N,N-dimethyl-formamide; toluene;

upstream raw materials:

2-Cyano-5-bromopyridine

3-trifluoromethyl-thiophenol

5-[[3-(trifluoromethyl)phenyl]sulfanyl]pyridin-2-carbonitrile

5-(3-(trifluoromethyl)phenylsulfonyl)picolinonitrile

Downstream raw materials:

1,3-dihydropyrrolo[3,4-c]pyridin-2-carboxylic acid [5-(3-trifluoromethylbenzenesulfonyl)pyridin-2-ylmethyl]amide