3-{[5-(5-chlorothiophen-2-yl)isoxazol-3-yl]methoxy}-2-nitrophenol

Base Information

• Chemical Name: 3-{[5-(5-chlorothiophen-2-yl)isoxazol-3-yl]methoxy}-2-nitrophenol
• CAS No.: 1402905-79-6
• Molecular Formula: C₁₄H₉ClN₂O₅S
• Molecular Weight: 352.755
• Mol file: 1402905-79-6.mol

Synonyms:3-{[5-(5-chlorothiophen-2-yl)isoxazol-3-yl]methoxy}-2-nitrophenol

Chemical Property of 3-{[5-(5-chlorothiophen-2-yl)isoxazol-3-yl]methoxy}-2-nitrophenol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-{[5-(5-chlorothiophen-2-yl)isoxazol-3-yl]methoxy}-2-nitrophenol

There total 1 articles about 3-{[5-(5-chlorothiophen-2-yl)isoxazol-3-yl]methoxy}-2-nitrophenol 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: 58.0%

2-nitroresorcinol (601-89-8) + 3-(bromomethyl)-5-(5-chlorothiophen-2-yl)isoxazole (323594-39-4) → 3-{[5-(5-chlorothiophen-2-yl)isoxazol-3-yl]methoxy}-2-nitrophenol (1402905-79-6)

Guidance literature:

2-nitroresorcinol; With potassium carbonate; In N,N-dimethyl-formamide; for 0.5h;

3-(bromomethyl)-5-(5-chlorothiophen-2-yl)isoxazole; In N,N-dimethyl-formamide; at 20 ℃;

DOI:10.1002/cmdc.201200224

Reference yield: 97.0%

(2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-(3-bromopropoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate (16977-81-4) + 3-{[5-(5-chlorothiophen-2-yl)isoxazol-3-yl]methoxy}-2-nitrophenol (1402905-79-6) → 3-(3-{[5-(5-chlorothiophen-2-yl)isoxazol-3-yl]methoxy}-2-nitrophenoxy)propyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside (1402905-80-9)

Guidance literature:

3-{[5-(5-chlorothiophen-2-yl)isoxazol-3-yl]methoxy}-2-nitrophenol; With potassium carbonate; In N,N-dimethyl-formamide; for 0.5h;

(2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-(3-bromopropoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate; In N,N-dimethyl-formamide; at 20 ℃;

DOI:10.1002/cmdc.201200224

Reference yield:

3-{[5-(5-chlorothiophen-2-yl)isoxazol-3-yl]methoxy}-2-nitrophenol (1402905-79-6) → 3-(2-amino-3-{[5-(5-chlorothiophen-2-yl)isoxazol-3-yl]methoxy}phenoxy)propyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside (1402905-81-0)

Guidance literature:

Multi-step reaction with 2 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 0.5 h

1.2: 20 °C

2.1: tin(II) chloride dihdyrate / ethyl acetate / 48 h / Reflux

With tin(II) chloride dihdyrate; potassium carbonate; In ethyl acetate; N,N-dimethyl-formamide;

DOI:10.1002/cmdc.201200224

upstream raw materials:

2-nitroresorcinol

3-(bromomethyl)-5-(5-chlorothiophen-2-yl)isoxazole

Downstream raw materials:

3-(2-amino-3-{[5-(5-chlorothiophen-2-yl)isoxazol-3-yl]methoxy}phenoxy)propyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

3-(2-amino-3-{[5-(5-chlorothien-2-yl)isoxazol-3-yl]methoxy}phenoxy)propyl β-D-glucopyranoside

3-(3-[1-(tert-butoxycarbonyl)piperidine-4-carboxamido]-2-{[5-(5-chlorothiophen-2-yl)isoxazol-3-yl]methoxy}phenoxy)propyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

3-(3-{[5-(5-chlorothiophen-2-yl)isoxazol-3-yl]methoxy}-2-(piperidine-4-carboxamido)phenoxy)propyl β-D-glucopyranoside