C₂₂H₂₂FN₃O₄

Base Information

Chemical Name:C₂₂H₂₂FN₃O₄
CAS No.:1279038-74-2
Molecular Formula:C₂₂H₂₂FN₃O₄
Molecular Weight:411.433
Hs Code.:

C<sub>22</sub>H<sub>22</sub>FN<sub>3</sub>O<sub>4</sub>

Synonyms:

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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 C₂₂H₂₂FN₃O₄

Chemical Property:

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Technology Process of C₂₂H₂₂FN₃O₄

There total 4 articles about C₂₂H₂₂FN₃O₄ 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:

: 736131-48-9,752198-38-2
(S)-3-amino-3-(2-methylphenyl)propionic acid

: 1318790-00-9
C₁₂H₁₁FN₂O₃

: 1279038-74-2
C₂₂H₂₂FN₃O₄

Guidance literature:: C₁₂H₁₁FN₂O₃; With O-<[cyano(ethoxycarbonyl)methylene]amino>-1,1,3,3-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 0.0833333h;

(S)-3-amino-3-(2-methylphenyl)propionic acid; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1021/jm300663n

Reference yield:

: 2924-15-4
(2-fluorophenyl)hydrazine hydrochloride

: 1279038-74-2
C₂₂H₂₂FN₃O₄

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine / methanol / 17 h / 0 - 20 °C

2.1: water; hydrogenchloride / ethyl acetate

3.1: caesium carbonate / N,N-dimethyl-formamide / 6 h / 50 °C

4.1: lithium hydroxide / methanol; water / 20 °C

5.1: N-ethyl-N,N-diisopropylamine; O-<[cyano(ethoxycarbonyl)methylene]amino>-1,1,3,3-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 0.08 h / 20 °C

5.2: 20 °C

With hydrogenchloride; O-<[cyano(ethoxycarbonyl)methylene]amino>-1,1,3,3-tetramethyluronium tetrafluoroborate; water; caesium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In methanol; water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm300663n

Reference yield:

: 1246555-84-9
methyl 1-(2-fluorophenyl)-5-hydroxy-1H-pyrazole-3-carboxylate

: 1279038-74-2
C₂₂H₂₂FN₃O₄

Guidance literature:: Multi-step reaction with 3 steps

1.1: caesium carbonate / N,N-dimethyl-formamide / 6 h / 50 °C

2.1: lithium hydroxide / methanol; water / 20 °C

3.1: N-ethyl-N,N-diisopropylamine; O-<[cyano(ethoxycarbonyl)methylene]amino>-1,1,3,3-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 0.08 h / 20 °C

3.2: 20 °C

With O-<[cyano(ethoxycarbonyl)methylene]amino>-1,1,3,3-tetramethyluronium tetrafluoroborate; caesium carbonate; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In methanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jm300663n