[5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl]-[3-(2-bromoethoxy)phenyl]methanone

Base Information

Chemical Name:[5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl]-[3-(2-bromoethoxy)phenyl]methanone
CAS No.:249937-22-2
Molecular Formula:C₁₈H₁₅BrFN₃O₂
Molecular Weight:404.238
Hs Code.:

Synonyms:[5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl]-[3-(2-bromoethoxy)phenyl]methanone

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Chemical Property of [5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl]-[3-(2-bromoethoxy)phenyl]methanone

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Technology Process of [5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl]-[3-(2-bromoethoxy)phenyl]methanone

There total 8 articles about [5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl]-[3-(2-bromoethoxy)phenyl]methanone 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:

: 249937-13-1
[5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl]-(3-hydroxyphenyl)methanone

: 540-51-2
2-bromoethanol

: 249937-22-2
[5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl]-[3-(2-bromoethoxy)phenyl]methanone

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In toluene;

Reference yield:

: 249937-13-1
[5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl]-(3-hydroxyphenyl)methanone

: 540-51-2
2-bromoethanol

: 249937-22-2
[5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl]-[3-(2-bromoethoxy)phenyl]methanone

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In toluene; at 20 ℃; for 16h;
DOI:10.1021/jm050736c

Reference yield:

: 249937-12-0
[5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl]-(3-methoxyphenyl)methanone

: 249937-22-2
[5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl]-[3-(2-bromoethoxy)phenyl]methanone

Guidance literature:: Multi-step reaction with 2 steps

1: BBr₃ / CH₂Cl₂ / 20 °C

2: 0.785 g / PPh₃; diethyl azodicarboxylate / toluene / 16 h / 20 °C

With boron tribromide; triphenylphosphine; diethylazodicarboxylate; In dichloromethane; toluene; 2: Mitsunobu coupling;
DOI:10.1021/jm050736c