C₂₉H₃₀N₈O₂

Base Information

Chemical Name:C₂₉H₃₀N₈O₂
CAS No.:1421373-60-5
Molecular Formula:C₂₉H₃₀N₈O₂
Molecular Weight:522.61
Hs Code.:

C<sub>29</sub>H<sub>30</sub>N<sub>8</sub>O<sub>2</sub>

Synonyms:C₂₉H₃₀N₈O₂

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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 C₂₉H₃₀N₈O₂

Chemical Property:

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Technology Process of C₂₉H₃₀N₈O₂

There total 9 articles about C₂₉H₃₀N₈O₂ 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: 48.0%

: 1421372-56-6
2-{[5-amino-2-methoxy-4-(4-methylpiperazin-1-yl)phenyl]amino}-4-(1-methylindol-3-yl)pyrimidine-5-carbonitrile

: 814-68-6,25189-84-8
acryloyl chloride

: 1421373-60-5
C₂₉H₃₀N₈O₂

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; for 1.5h; Cooling with ice;

Reference yield:

: 937366-57-9
3-(2,5-dichloropyrimidine-4-yl)-1H-indole

: 1421373-60-5
C₂₉H₃₀N₈O₂

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydride / tetrahydrofuran / 0.42 h / 0 °C / Inert atmosphere

1.2: 2 h / 0 - 20 °C / Inert atmosphere

2.1: toluene-4-sulfonic acid / 18 h / 125 °C

3.1: 2,2,2-trifluoroethanol / 1.5 h / 120 - 140 °C / Microwave irradiation

4.1: iron; ammonium chloride / water; ethanol / 4 h / Reflux

5.1: zinc; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / N,N-dimethyl acetamide / 2 h / 95 °C / Inert atmosphere

6.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 1.5 h / Cooling with ice

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; iron; sodium hydride; ammonium chloride; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; zinc; XPhos; In tetrahydrofuran; ethanol; dichloromethane; 2,2,2-trifluoroethanol; N,N-dimethyl acetamide; water;

Reference yield:

: 1075705-01-9
4-fluoro-2-methoxy-5-nitro-phenylamine

: 1421373-60-5
C₂₉H₃₀N₈O₂

Guidance literature:: Multi-step reaction with 5 steps

1: toluene-4-sulfonic acid / 18 h / 125 °C

2: 2,2,2-trifluoroethanol / 1.5 h / 120 - 140 °C / Microwave irradiation

3: iron; ammonium chloride / water; ethanol / 4 h / Reflux

4: zinc; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / N,N-dimethyl acetamide / 2 h / 95 °C / Inert atmosphere

5: N-ethyl-N,N-diisopropylamine / dichloromethane / 1.5 h / Cooling with ice

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; iron; ammonium chloride; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; zinc; XPhos; In ethanol; dichloromethane; 2,2,2-trifluoroethanol; N,N-dimethyl acetamide; water;