[5-(4',5'-Difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzo[d] isoxazol-3-yl]-methyl-amine

Base Information

Chemical Name:[5-(4',5'-Difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzo[d] isoxazol-3-yl]-methyl-amine
CAS No.:1299489-67-0
Molecular Formula:C₂₂H₁₈F₂N₂O₃
Molecular Weight:396.393
Hs Code.:

Synonyms:[5-(4',5'-Difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzo[d] isoxazol-3-yl]-methyl-amine

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Chemical Property of [5-(4',5'-Difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzo[d] isoxazol-3-yl]-methyl-amine

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Technology Process of [5-(4',5'-Difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzo[d] isoxazol-3-yl]-methyl-amine

There total 9 articles about [5-(4',5'-Difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzo[d] isoxazol-3-yl]-methyl-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:

: 1299489-70-5
[5-(4',5'-difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzo[d]isoxazol-3-yl]-carbamic acid tert-butyl ester

: 77-78-1
dimethyl sulfate

: 1299489-67-0
[5-(4',5'-Difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzo[d] isoxazol-3-yl]-methyl-amine

Guidance literature:: [5-(4',5'-difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzo[d]isoxazol-3-yl]-carbamic acid tert-butyl ester; dimethyl sulfate; With potassium carbonate; for 6h;

With trifluoroacetic acid; In dichloromethane; for 1h;

Reference yield:

: 64113-84-4
2-fluoro-5-methylbenzonitrile

: 1299489-67-0
[5-(4',5'-Difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzo[d] isoxazol-3-yl]-methyl-amine

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium tert-butylate / tetrahydrofuran / 20 °C / Reflux

1.2: 2 h / Reflux

1.3: pH 12

2.1: dmap / dichloromethane / 20 °C

3.1: 2,2'-azobis(isobutyronitrile); N-Bromosuccinimide / tetrachloromethane / 3 h / Reflux

4.1: potassium carbonate / N,N-dimethyl-formamide; tetrahydrofuran

5.1: hydrazine hydrate / ethanol / 3.5 h

6.1: potassium carbonate / 6 h

6.2: 1 h

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); potassium tert-butylate; potassium carbonate; hydrazine hydrate; dmap; In tetrahydrofuran; tetrachloromethane; ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 540-38-5
p-Iodophenol

: 1299489-67-0
[5-(4',5'-Difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzo[d] isoxazol-3-yl]-methyl-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide; water / 1 h / 80 - 85 °C / Inert atmosphere

2.1: potassium carbonate / N,N-dimethyl-formamide; tetrahydrofuran

3.1: hydrazine hydrate / ethanol / 3.5 h

4.1: potassium carbonate / 6 h

4.2: 1 h

With potassium carbonate; hydrazine hydrate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide;