C₁₇H₁₇N₃

Base Information

Chemical Name:C₁₇H₁₇N₃
CAS No.:861806-27-1
Molecular Formula:C₁₇H₁₇N₃
Molecular Weight:263.342
Hs Code.:

C<sub>17</sub>H<sub>17</sub>N<sub>3</sub>

Synonyms:C₁₇H₁₇N₃

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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 C₁₇H₁₇N₃

Chemical Property:

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Technology Process of C₁₇H₁₇N₃

There total 3 articles about C₁₇H₁₇N₃ 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: 82.0%

: 137596-50-0
1-methyl-2,5-bis(4-nitrophenyl)pyrrole

: 861806-27-1
C₁₇H₁₇N₃

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; at 20 ℃; for 6h; under 2585.74 Torr;
DOI:10.1515/HC.2004.10.6.423

Reference yield:

: 96-54-8
N-Methylpyrrole

: 861806-27-1
C₁₇H₁₇N₃

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-BuLi; tetramethylethylenediamine / hexane / 1 h / Heating

1.2: (n-Bu)3SnCl / hexane / 2 h / Heating

1.3: (PPh₃)4Pd / dioxane / 90 - 100 °C

2.1: aq. SnCl₂ / ethyl acetate / Heating

With n-butyllithium; N,N,N,N,-tetramethylethylenediamine; tin(ll) chloride; In hexane; ethyl acetate; 1.3: Stille coupling;
DOI:10.1016/j.bmcl.2005.05.080

Reference yield:

: 586-78-7
para-nitrophenyl bromide

: 861806-27-1
C₁₇H₁₇N₃

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-BuLi; tetramethylethylenediamine / hexane / 1 h / Heating

1.2: (n-Bu)3SnCl / hexane / 2 h / Heating

1.3: (PPh₃)4Pd / dioxane / 90 - 100 °C

2.1: aq. SnCl₂ / ethyl acetate / Heating

With n-butyllithium; N,N,N,N,-tetramethylethylenediamine; tin(ll) chloride; In hexane; ethyl acetate; 1.3: Stille coupling;
DOI:10.1016/j.bmcl.2005.05.080