(4-fluorophenyl)(3-(phenoxymethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)methanone

Base Information

Chemical Name:(4-fluorophenyl)(3-(phenoxymethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)methanone
CAS No.:1384873-32-8
Molecular Formula:C₂₂H₁₉FN₂O₂
Molecular Weight:362.403
Hs Code.:

Synonyms:(4-fluorophenyl)(3-(phenoxymethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)methanone

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (4-fluorophenyl)(3-(phenoxymethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)methanone

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Technology Process of (4-fluorophenyl)(3-(phenoxymethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)methanone

There total 6 articles about (4-fluorophenyl)(3-(phenoxymethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)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: 69.0%

: 1384873-55-5
(4-fluorophenyl)(3-(hydroxymethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)methanone

: 108-95-2,27073-41-2
phenol

: 1384873-32-8
(4-fluorophenyl)(3-(phenoxymethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)methanone

Guidance literature:: With di-isopropyl azodicarboxylate; In tetrahydrofuran; at 20 ℃; for 16h; Inert atmosphere;
DOI:10.1021/jm500259z

Reference yield:

: 1384873-49-7
(3-bromo-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)(4-fluorophenyl)methanone

: 1384873-32-8
(4-fluorophenyl)(3-(phenoxymethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / toluene / 1 h / 120 °C

2.1: ozone / dichloromethane; methanol / 20 °C / Cooling with acetone-dry ice

2.2: 1 h

3.1: di-isopropyl azodicarboxylate / tetrahydrofuran / 20 °C

With di-isopropyl azodicarboxylate; ozone; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; methanol; dichloromethane; toluene; 1.1: Stille Coupling / 3.1: Mitsunobu reaction;

Reference yield:

: 456-22-4
4-Fluorobenzoic acid

: 1384873-32-8
(4-fluorophenyl)(3-(phenoxymethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 20 °C

2.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / toluene / 1 h / 120 °C

3.1: ozone / dichloromethane; methanol / 20 °C / Cooling with acetone-dry ice

3.2: 1 h

4.1: di-isopropyl azodicarboxylate / tetrahydrofuran / 20 °C

With di-isopropyl azodicarboxylate; ozone; N-ethyl-N,N-diisopropylamine; HATU; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; toluene; 2.1: Stille Coupling / 4.1: Mitsunobu reaction;