2-amino-9-bromomethyl-4-(4-fluoro-phenyl)-indeno[1,2-d]pyrimidin-5-one

Base Information

Chemical Name:2-amino-9-bromomethyl-4-(4-fluoro-phenyl)-indeno[1,2-d]pyrimidin-5-one
CAS No.:1297598-97-0
Molecular Formula:C₁₈H₁₁BrFN₃O
Molecular Weight:384.207
Hs Code.:

Synonyms:2-amino-9-bromomethyl-4-(4-fluoro-phenyl)-indeno[1,2-d]pyrimidin-5-one

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Chemical Property of 2-amino-9-bromomethyl-4-(4-fluoro-phenyl)-indeno[1,2-d]pyrimidin-5-one

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Technology Process of 2-amino-9-bromomethyl-4-(4-fluoro-phenyl)-indeno[1,2-d]pyrimidin-5-one

There total 7 articles about 2-amino-9-bromomethyl-4-(4-fluoro-phenyl)-indeno[1,2-d]pyrimidin-5-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:

: 1297598-96-9
[9-bromomethyl-4-(4-fluorophenyl)-5-oxo-5H-indeno[1,2-d]pyrimidin-2-yl]-bis-carbamic acid tert-butyl ester

: 1297598-97-0
2-amino-9-bromomethyl-4-(4-fluoro-phenyl)-indeno[1,2-d]pyrimidin-5-one

Guidance literature:: [9-bromomethyl-4-(4-fluorophenyl)-5-oxo-5H-indeno[1,2-d]pyrimidin-2-yl]-bis-carbamic acid tert-butyl ester; With trifluoroacetic acid; In dichloromethane; for 2h;

With sodium hydrogencarbonate; In water;

Reference yield:

: 1297598-92-5
2-(4-fluorobenzylidene)-7-methylindan-1-one

: 1297598-97-0
2-amino-9-bromomethyl-4-(4-fluoro-phenyl)-indeno[1,2-d]pyrimidin-5-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydroxide / ethanol / 0.5 h

1.2: Reflux

2.1: sodium hydroxide; oxygen / 1-methyl-pyrrolidin-2-one / 16 h / 80 °C

3.1: dmap / tetrahydrofuran / 4 h

4.1: dibenzoyl peroxide; 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione / benzene / 16 h / Reflux

5.1: trifluoroacetic acid / dichloromethane / 2 h

With dmap; 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; oxygen; trifluoroacetic acid; sodium hydroxide; dibenzoyl peroxide; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; ethanol; dichloromethane; benzene;

Reference yield:

: 459-57-4
4-fluorobenzaldehyde

: 1297598-97-0
2-amino-9-bromomethyl-4-(4-fluoro-phenyl)-indeno[1,2-d]pyrimidin-5-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydroxide / ethanol; water / 1.5 h

2.1: sodium hydroxide / ethanol / 0.5 h

2.2: Reflux

3.1: sodium hydroxide; oxygen / 1-methyl-pyrrolidin-2-one / 16 h / 80 °C

4.1: dmap / tetrahydrofuran / 4 h

5.1: dibenzoyl peroxide; 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione / benzene / 16 h / Reflux

6.1: trifluoroacetic acid / dichloromethane / 2 h

With dmap; 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; oxygen; trifluoroacetic acid; sodium hydroxide; dibenzoyl peroxide; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; ethanol; dichloromethane; water; benzene;