C₁₉H₂₂N₆O₂S

Base Information

Chemical Name:C₁₉H₂₂N₆O₂S
CAS No.:1418002-46-6
Molecular Formula:C₁₉H₂₂N₆O₂S
Molecular Weight:398.489
Hs Code.:

C<sub>19</sub>H<sub>22</sub>N<sub>6</sub>O<sub>2</sub>S

Synonyms:C₁₉H₂₂N₆O₂S

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Chemical Property of C₁₉H₂₂N₆O₂S

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Technology Process of C₁₉H₂₂N₆O₂S

There total 8 articles about C₁₉H₂₂N₆O₂S 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: 54.0%

: 1418003-25-4
trans-[4-(2-aminomethyl-1,3,5,9-tetraaza-cyclopenta[a]naphthalen-1-yl)-cyclohexyl]-acetonitrile

: 124-63-0
methanesulfonyl chloride

: 1418002-46-6
C₁₉H₂₂N₆O₂S

Guidance literature:: With triethylamine; In tetrahydrofuran; at 0 ℃; for 0.166667h;

Reference yield:

: 239074-29-4
trans (4-hydroxymethyl-cyclohexyl)-carbamic acid tert-butyl ester

: 1418002-46-6
C₁₉H₂₂N₆O₂S

Guidance literature:: Multi-step reaction with 8 steps

1.1: pyridine / dichloromethane / 5 h / 0 - 20 °C

2.1: dimethyl sulfoxide / 4 h / 90 °C

3.1: trifluoroacetic acid / dichloromethane / 2.5 h / 20 °C

4.1: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 0.33 h / 120 °C / Microwave irradiation

5.1: ammonium chloride; iron / ethanol; water / 8.75 h / 80 °C

6.1: triethyloxonium fluoroborate / dichloromethane / 2 h / 20 °C

6.2: 19 h / 20 - 75 °C

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

8.1: triethylamine / tetrahydrofuran / 0.17 h / 0 °C

With pyridine; hydrogenchloride; triethyloxonium fluoroborate; iron; ammonium chloride; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; dimethyl sulfoxide; isopropyl alcohol;

Reference yield:

: 683269-95-6
N-[trans-4-[[(methylsulfonyl)oxy]methyl]cyclohexyl]carbamic acid tert-butyl ester

: 1418002-46-6
C₁₉H₂₂N₆O₂S

Guidance literature:: Multi-step reaction with 7 steps

1.1: dimethyl sulfoxide / 4 h / 90 °C

2.1: trifluoroacetic acid / dichloromethane / 2.5 h / 20 °C

3.1: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 0.33 h / 120 °C / Microwave irradiation

4.1: ammonium chloride; iron / ethanol; water / 8.75 h / 80 °C

5.1: triethyloxonium fluoroborate / dichloromethane / 2 h / 20 °C

5.2: 19 h / 20 - 75 °C

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

7.1: triethylamine / tetrahydrofuran / 0.17 h / 0 °C

With hydrogenchloride; triethyloxonium fluoroborate; iron; ammonium chloride; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; dimethyl sulfoxide; isopropyl alcohol;