(1R,2S)-1-((1-(4-fluorophenyl)-1H-indazol-5-yl)oxy)-1-(3-methoxyphenyl)propan-2-amine

Base Information

• Chemical Name: (1R,2S)-1-((1-(4-fluorophenyl)-1H-indazol-5-yl)oxy)-1-(3-methoxyphenyl)propan-2-amine
• CAS No.: 1034153-23-5
• Molecular Formula: C₂₃H₂₂FN₃O₂
• Molecular Weight: 391.445
• Mol file: 1034153-23-5.mol

Synonyms:(1R,2S)-1-((1-(4-fluorophenyl)-1H-indazol-5-yl)oxy)-1-(3-methoxyphenyl)propan-2-amine

Chemical Property of (1R,2S)-1-((1-(4-fluorophenyl)-1H-indazol-5-yl)oxy)-1-(3-methoxyphenyl)propan-2-amine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (1R,2S)-1-((1-(4-fluorophenyl)-1H-indazol-5-yl)oxy)-1-(3-methoxyphenyl)propan-2-amine

There total 4 articles about (1R,2S)-1-((1-(4-fluorophenyl)-1H-indazol-5-yl)oxy)-1-(3-methoxyphenyl)propan-2-amine 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: 77.0%

1-(4-fluorophenyl)-5-iodo-1H-indazole (1025762-98-4) + (1R,2S)-2-amino-1-(3-methoxyphenyl)propan-1-ol hydrochloride (1034156-00-7) → (1R,2S)-1-((1-(4-fluorophenyl)-1H-indazol-5-yl)oxy)-1-(3-methoxyphenyl)propan-2-amine (1034153-23-5)

Guidance literature:

With copper(l) iodide; caesium carbonate; at 120 ℃; for 10h; Inert atmosphere;

DOI:10.1021/ol501432h

Reference yield: 38.0%

1-(fluorophenyl)-5-iodo-1H-indazole + (1R,2S)-norephedrine (492-41-1,58550-13-3,757124-50-8) → (1R,2S)-1-((1-(4-fluorophenyl)-1H-indazol-5-yl)oxy)-1-(3-methoxyphenyl)propan-2-amine (1034153-23-5)

Guidance literature:

With caesium carbonate; copper(l) iodide; In propyl cyanide; at 125 ℃; for 5h;

Reference yield:

1-(3-methoxyphenyl)-2-nitropropan-1-ol → (1R,2S)-1-((1-(4-fluorophenyl)-1H-indazol-5-yl)oxy)-1-(3-methoxyphenyl)propan-2-amine (1034153-23-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 10 wt% Pd(OH)2 on carbon; hydrogen / methanol / 4 h / 20 °C / Inert atmosphere

2: copper(l) iodide; caesium carbonate / 10 h / 120 °C / Inert atmosphere

With copper(l) iodide; 10 wt% Pd(OH)2 on carbon; hydrogen; caesium carbonate; In methanol;

DOI:10.1021/ol501432h

upstream raw materials:

(1R,2S)-norephedrine

1-(4-fluorophenyl)-5-iodo-1H-indazole

(1R,2S)-2-amino-1-(3-methoxyphenyl)propan-1-ol hydrochloride

2-Fluoro-5-iodo-benzaldehyde

Downstream raw materials:

N-[[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]carbamoylmethyl]acetamide

N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]cyclopentanecarboxamide

(2R)-N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]-2-hydroxy-propanamide

N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]oxamide