2-[(E)-3-(2-fluoro-5-methoxy-phenyl)allylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester

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Chemical Name:2-[(E)-3-(2-fluoro-5-methoxy-phenyl)allylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester
CAS No.:1400705-81-8
Molecular Formula:C₁₉H₂₂FN₃O₃
Molecular Weight:359.4
Hs Code.:

Synonyms:2-[(E)-3-(2-fluoro-5-methoxy-phenyl)allylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester

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Chemical Property of 2-[(E)-3-(2-fluoro-5-methoxy-phenyl)allylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester

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Technology Process of 2-[(E)-3-(2-fluoro-5-methoxy-phenyl)allylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester

There total 7 articles about 2-[(E)-3-(2-fluoro-5-methoxy-phenyl)allylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester 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: 47.0%

: 1400705-69-2
4,6-dimethyl-2-[(E)-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)allylamino]pyrimidine-5-carboxylic acid ethyl ester

: 2-bromo-1-fluoro-4-methoxy-benzene

: 1400705-81-8
2-[(E)-3-(2-fluoro-5-methoxy-phenyl)allylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester

Guidance literature:: With cesium fluoride; bis-triphenylphosphine-palladium(II) chloride; monophosphine 1,2,3,4,5-pentaphenyl-1'-(di-tert-butylphosphino)ferrocene; In tetrahydrofuran; at 120 ℃; for 0.333333h; microwave irradiation; Inert atmosphere;

Reference yield:

: 141-97-9
ethyl acetoacetate

: 1400705-81-8
2-[(E)-3-(2-fluoro-5-methoxy-phenyl)allylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: acetic acid / ethanol / 90 °C

2.1: nitric acid / 0.25 h / 0 °C

2.2: Cooling with ice

3.1: N-ethyl-N,N-diisopropylamine; trichlorophosphate / 2 h / 110 °C

4.1: ethanol / 1 h / 160 °C / microwave irradiation

4.2: 20 °C

5.1: triethylamine / Schwartz's reagent / tetrahydrofuran / 20.3 h / 150 °C / microwave irradiation

6.1: cesium fluoride / bis-triphenylphosphine-palladium(II) chloride; monophosphine 1,2,3,4,5-pentaphenyl-1'-(di-tert-butylphosphino)ferrocene / tetrahydrofuran / 0.33 h / 120 °C / microwave irradiation; Inert atmosphere

With nitric acid; triethylamine; N-ethyl-N,N-diisopropylamine; cesium fluoride; trichlorophosphate; bis-triphenylphosphine-palladium(II) chloride; Schwartz's reagent; monophosphine 1,2,3,4,5-pentaphenyl-1'-(di-tert-butylphosphino)ferrocene; acetic acid; In tetrahydrofuran; ethanol;

Reference yield:

: 406482-19-7
2-fluoro-5-methoxyphenylboronic acid

: 1400705-81-8
2-[(E)-3-(2-fluoro-5-methoxy-phenyl)allylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: copper(ll) bromide / water; methanol / Reflux

2: cesium fluoride / bis-triphenylphosphine-palladium(II) chloride; monophosphine 1,2,3,4,5-pentaphenyl-1'-(di-tert-butylphosphino)ferrocene / tetrahydrofuran / 0.33 h / 120 °C / microwave irradiation; Inert atmosphere

With cesium fluoride; copper(ll) bromide; bis-triphenylphosphine-palladium(II) chloride; monophosphine 1,2,3,4,5-pentaphenyl-1'-(di-tert-butylphosphino)ferrocene; In tetrahydrofuran; methanol; water;