6-(1-benzhydryl-3-methylazetidin-3-ylamino)-7-fluoro-4-methyl-2,10-dihydro-9-oxa-1,2,4a-triazaphenanthren-3-one

Base Information

Chemical Name:6-(1-benzhydryl-3-methylazetidin-3-ylamino)-7-fluoro-4-methyl-2,10-dihydro-9-oxa-1,2,4a-triazaphenanthren-3-one
CAS No.:1613720-40-3
Molecular Formula:C₂₈H₂₈FN₅O₂
Molecular Weight:485.561
Hs Code.:

Synonyms:6-(1-benzhydryl-3-methylazetidin-3-ylamino)-7-fluoro-4-methyl-2,10-dihydro-9-oxa-1,2,4a-triazaphenanthren-3-one

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Chemical Property of 6-(1-benzhydryl-3-methylazetidin-3-ylamino)-7-fluoro-4-methyl-2,10-dihydro-9-oxa-1,2,4a-triazaphenanthren-3-one

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Technology Process of 6-(1-benzhydryl-3-methylazetidin-3-ylamino)-7-fluoro-4-methyl-2,10-dihydro-9-oxa-1,2,4a-triazaphenanthren-3-one

There total 7 articles about 6-(1-benzhydryl-3-methylazetidin-3-ylamino)-7-fluoro-4-methyl-2,10-dihydro-9-oxa-1,2,4a-triazaphenanthren-3-one 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: 28.0%

: 1613719-91-7
6-amino-7-fluoro-4-methyl-2,10-dihydro-9-oxa-1,2,4a-triazaphenanthren-3-one

: 133891-87-9
methanesulfonic acid 1-benzhydryl-3-methylazetidin-3-yl ester

: 1613720-40-3
6-(1-benzhydryl-3-methylazetidin-3-ylamino)-7-fluoro-4-methyl-2,10-dihydro-9-oxa-1,2,4a-triazaphenanthren-3-one

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 80 ℃;

Reference yield:

: 53981-24-1
2-amino-5-fluorophenol

: 1613720-40-3
6-(1-benzhydryl-3-methylazetidin-3-ylamino)-7-fluoro-4-methyl-2,10-dihydro-9-oxa-1,2,4a-triazaphenanthren-3-one

Guidance literature:: Multi-step reaction with 7 steps

1.1: tetra-N-butylammonium tribromide; potassium carbonate / acetonitrile / Reflux

2.1: sulfuric acid; nitric acid / 0.17 h / -10 °C

3.1: potassium carbonate / acetone / 0.25 h / 20 °C

3.2: 5 h / Reflux

4.1: Lawessons reagent / toluene / 3 h / Reflux

5.1: zinc; ammonium chloride / methanol; tetrahydrofuran / 3 h / Reflux

6.1: hydrazine / ethanol / 2 h / 90 °C

7.1: potassium carbonate / N,N-dimethyl-formamide / 80 °C

With Lawessons reagent; sulfuric acid; nitric acid; tetra-N-butylammonium tribromide; potassium carbonate; ammonium chloride; hydrazine; zinc; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; acetone; toluene; acetonitrile;

Reference yield:

: 103361-99-5
7-fluoro-3,4-dihydro-3-oxo-2H-1,4-benzoxazine

: 1613720-40-3
6-(1-benzhydryl-3-methylazetidin-3-ylamino)-7-fluoro-4-methyl-2,10-dihydro-9-oxa-1,2,4a-triazaphenanthren-3-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: sulfuric acid; nitric acid / 0.17 h / -10 °C

2.1: potassium carbonate / acetone / 0.25 h / 20 °C

2.2: 5 h / Reflux

3.1: Lawessons reagent / toluene / 3 h / Reflux

4.1: zinc; ammonium chloride / methanol; tetrahydrofuran / 3 h / Reflux

5.1: hydrazine / ethanol / 2 h / 90 °C

6.1: potassium carbonate / N,N-dimethyl-formamide / 80 °C

With Lawessons reagent; sulfuric acid; nitric acid; potassium carbonate; ammonium chloride; hydrazine; zinc; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; acetone; toluene;