C₁₇H₁₈ClN₅O

Base Information

Chemical Name:C₁₇H₁₈ClN₅O
CAS No.:1415583-73-1
Molecular Formula:C₁₇H₁₈ClN₅O
Molecular Weight:343.816
Hs Code.:

C<sub>17</sub>H<sub>18</sub>ClN<sub>5</sub>O

Synonyms:C₁₇H₁₈ClN₅O

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Chemical Property of C₁₇H₁₈ClN₅O

Chemical Property:

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Technology Process of C₁₇H₁₈ClN₅O

There total 5 articles about C₁₇H₁₈ClN₅O 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:

: 1415583-55-9
C₁₆H₁₂N₄O₂

: 1415583-73-1
C₁₇H₁₈ClN₅O

Guidance literature:: Multi-step reaction with 4 steps

1: N-ethyl-N,N-diisopropylamine; trichlorophosphate / 1 h / Reflux

2: N-ethyl-N,N-diisopropylamine / butan-1-ol; isopropyl alcohol / Reflux

3: tetrabutyl-ammonium chloride; ammonium formate / palladium 10% on activated carbon / water; tetrahydrofuran; methanol / 2.5 h / 60 °C

4: hydrogenchloride / methanol / 20 °C

With hydrogenchloride; tetrabutyl-ammonium chloride; ammonium formate; N-ethyl-N,N-diisopropylamine; trichlorophosphate; palladium 10% on activated carbon; In tetrahydrofuran; methanol; water; isopropyl alcohol; butan-1-ol;

Reference yield:

: 1415583-56-0
2-phenyl-4,6-dichloro-5-phenylazopyrimidine

: 1415583-73-1
C₁₇H₁₈ClN₅O

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / butan-1-ol; isopropyl alcohol / Reflux

2: tetrabutyl-ammonium chloride; ammonium formate / palladium 10% on activated carbon / water; tetrahydrofuran; methanol / 2.5 h / 60 °C

3: hydrogenchloride / methanol / 20 °C

With hydrogenchloride; tetrabutyl-ammonium chloride; ammonium formate; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; In tetrahydrofuran; methanol; water; isopropyl alcohol; butan-1-ol;

Reference yield:

: 1670-14-0
benzamidine monohydrochloride

: 1415583-73-1
C₁₇H₁₈ClN₅O

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium methylate / methanol / 2 h / 55 °C

1.2: 0.5 h

2.1: hydrogenchloride; sodium nitrite / water

2.2: 0.5 h

3.1: N-ethyl-N,N-diisopropylamine; trichlorophosphate / 1 h / Reflux

4.1: N-ethyl-N,N-diisopropylamine / butan-1-ol; isopropyl alcohol / Reflux

5.1: tetrabutyl-ammonium chloride; ammonium formate / palladium 10% on activated carbon / water; tetrahydrofuran; methanol / 2.5 h / 60 °C

6.1: hydrogenchloride / methanol / 20 °C

With hydrogenchloride; tetrabutyl-ammonium chloride; ammonium formate; sodium methylate; N-ethyl-N,N-diisopropylamine; sodium nitrite; trichlorophosphate; palladium 10% on activated carbon; In tetrahydrofuran; methanol; water; isopropyl alcohol; butan-1-ol;