C₂₂H₂₂FN₇O

Base Information

Chemical Name:C₂₂H₂₂FN₇O
CAS No.:1613021-22-9
Molecular Formula:C₂₂H₂₂FN₇O
Molecular Weight:419.461
Hs Code.:

C<sub>22</sub>H<sub>22</sub>FN<sub>7</sub>O

Synonyms:C₂₂H₂₂FN₇O

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Chemical Property of C₂₂H₂₂FN₇O

Chemical Property:

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Technology Process of C₂₂H₂₂FN₇O

There total 8 articles about C₂₂H₂₂FN₇O 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:

: 1552231-28-3
1-(4-fluorophenyl)-1,2,4-triazole-3-carboxylic acid

: (3S)-1-(3-ethylpyrrolo[1,2-a]pyrazin-1-yl)pyrrolidin-3-amine dihydrochloride

: 1613021-22-9
C₂₂H₂₂FN₇O

Guidance literature:: With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In dimethyl sulfoxide; for 0.833333h;

Reference yield:

: 35302-72-8
pyrrol-2-yl trichloromethyl ketone

: 1613021-22-9
C₂₂H₂₂FN₇O

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / acetone / 19 h / 20 °C

2: ammonium acetate / acetic acid / 3 h / 160 °C / Sealed tube

3: trichlorophosphate / 0.33 h / 80 °C

4: N-ethyl-N,N-diisopropylamine; 1-butyl-3-methylimidazolium Tetrafluoroborate / 1-methyl-pyrrolidin-2-one / 2.08 h / 110 °C

5: hydrogenchloride / 1,4-dioxane / 0.5 h / 50 °C

6: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; triethylamine / dimethyl sulfoxide / 0.83 h

With hydrogenchloride; ammonium acetate; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; 1-butyl-3-methylimidazolium Tetrafluoroborate; trichlorophosphate; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; acetic acid; dimethyl sulfoxide; acetone;

Reference yield:

: 1613023-10-1
3-ethylpyrrolo[1,2-a]pyrazin-1(2H)-one

: 1613021-22-9
C₂₂H₂₂FN₇O

Guidance literature:: Multi-step reaction with 4 steps

1: trichlorophosphate / 0.33 h / 80 °C

2: N-ethyl-N,N-diisopropylamine; 1-butyl-3-methylimidazolium Tetrafluoroborate / 1-methyl-pyrrolidin-2-one / 2.08 h / 110 °C

3: hydrogenchloride / 1,4-dioxane / 0.5 h / 50 °C

4: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; triethylamine / dimethyl sulfoxide / 0.83 h

With hydrogenchloride; triethylamine; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; 1-butyl-3-methylimidazolium Tetrafluoroborate; trichlorophosphate; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; dimethyl sulfoxide;