(E)-(S)-2-amino-7-(4-fluoro-2-(pyridin-3-yl)phenyl)-4-methyl-7,8-dihydro-6H-quinazolin-5-one O-(2-(azetidin-1-yl)ethyl)oxime

Base Information

Chemical Name:(E)-(S)-2-amino-7-(4-fluoro-2-(pyridin-3-yl)phenyl)-4-methyl-7,8-dihydro-6H-quinazolin-5-one O-(2-(azetidin-1-yl)ethyl)oxime
CAS No.:1433608-04-8
Molecular Formula:C₂₅H₂₇FN₆O
Molecular Weight:446.527
Hs Code.:

Synonyms:(E)-(S)-2-amino-7-(4-fluoro-2-(pyridin-3-yl)phenyl)-4-methyl-7,8-dihydro-6H-quinazolin-5-one O-(2-(azetidin-1-yl)ethyl)oxime

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Chemical Property of (E)-(S)-2-amino-7-(4-fluoro-2-(pyridin-3-yl)phenyl)-4-methyl-7,8-dihydro-6H-quinazolin-5-one O-(2-(azetidin-1-yl)ethyl)oxime

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Technology Process of (E)-(S)-2-amino-7-(4-fluoro-2-(pyridin-3-yl)phenyl)-4-methyl-7,8-dihydro-6H-quinazolin-5-one O-(2-(azetidin-1-yl)ethyl)oxime

There total 7 articles about (E)-(S)-2-amino-7-(4-fluoro-2-(pyridin-3-yl)phenyl)-4-methyl-7,8-dihydro-6H-quinazolin-5-one O-(2-(azetidin-1-yl)ethyl)oxime 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: 33.0%

: 503-29-7
azetidine

: 1433608-19-5
(E)-(S)-2-(((2-amino-7-(4-fluoro-2-(pyridin-3-yl)phenyl)-4-methyl-7,8-dihydro-6H-quinazolin-5-ylidene)amino)oxy)ethyl methansulfonate

: 1433608-04-8
(E)-(S)-2-amino-7-(4-fluoro-2-(pyridin-3-yl)phenyl)-4-methyl-7,8-dihydro-6H-quinazolin-5-one O-(2-(azetidin-1-yl)ethyl)oxime

Guidance literature:: In acetonitrile; at 50 ℃; for 2.5h; Heating; Microwave irradiation;

Reference yield:

: 1433605-21-0
(E)-2-amino-7-(4-fluoro-2-(pyridin-3-yl)phenyl)-4-methyl-7,8-dihydro-6H-quinazolin-5-one oxime

: 1433608-04-8
(E)-(S)-2-amino-7-(4-fluoro-2-(pyridin-3-yl)phenyl)-4-methyl-7,8-dihydro-6H-quinazolin-5-one O-(2-(azetidin-1-yl)ethyl)oxime

Guidance literature:: Multi-step reaction with 6 steps

1: triethylamine / N,N-dimethyl-formamide / 0 - 20 °C

2: methanol; sodium hydroxide / 0.25 h / 20 °C

3: sodium hydride / N,N-dimethyl-formamide; mineral oil / 2 h / 20 °C / Inert atmosphere

4: hydrogenchloride / dichloromethane; 1,4-dioxane / 2 h / 20 °C

5: triethylamine / N,N-dimethyl-formamide; dichloromethane / 2 h / 20 °C

6: acetonitrile / 2.5 h / 50 °C / Heating; Microwave irradiation

With hydrogenchloride; methanol; sodium hydride; triethylamine; sodium hydroxide; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; acetonitrile; mineral oil;

Reference yield:

: (E)-2-amino-7-(4-fluoro-2-(pyridin-3-yl)phenyl)-4-methyl-7,8-dihydro-6H-quinazolin-5-one O-acetyl oxime

: 1433608-04-8
(E)-(S)-2-amino-7-(4-fluoro-2-(pyridin-3-yl)phenyl)-4-methyl-7,8-dihydro-6H-quinazolin-5-one O-(2-(azetidin-1-yl)ethyl)oxime

Guidance literature:: Multi-step reaction with 5 steps

1: butan-1-ol / tetrahydrofuran / 36 h / 30 °C / Enzymatic reaction

2: sodium hydride / N,N-dimethyl-formamide; mineral oil / 2 h / 20 °C / Inert atmosphere

3: hydrogenchloride / dichloromethane; 1,4-dioxane / 2 h / 20 °C

4: triethylamine / N,N-dimethyl-formamide; dichloromethane / 2 h / 20 °C

5: acetonitrile / 2.5 h / 50 °C / Heating; Microwave irradiation

With hydrogenchloride; sodium hydride; triethylamine; butan-1-ol; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; acetonitrile; mineral oil;