C₂₉H₂₅N₇O₄

Base Information

Chemical Name:C₂₉H₂₅N₇O₄
CAS No.:1301141-72-9
Molecular Formula:C₂₉H₂₅N₇O₄
Molecular Weight:535.562
Hs Code.:

C<sub>29</sub>H<sub>25</sub>N<sub>7</sub>O<sub>4</sub>

Synonyms:C₂₉H₂₅N₇O₄

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Chemical Property of C₂₉H₂₅N₇O₄

Chemical Property:

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Technology Process of C₂₉H₂₅N₇O₄

There total 10 articles about C₂₉H₂₅N₇O₄ 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:

: 38870-89-2
Methoxyacetyl chloride

: 1301141-68-3
C₂₆H₂₁N₇O₂

: 1301141-72-9
C₂₉H₂₅N₇O₄

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃;

Reference yield:

: 2227-64-7
3'-nitro-2-bromoacetophenone

: 1301141-72-9
C₂₉H₂₅N₇O₄

Guidance literature:: Multi-step reaction with 9 steps

1.1: sodium hydrogencarbonate / ethanol / 4 h / 20 °C

2.1: N-iodo-succinimide / N,N-dimethyl-formamide / 4 h / 20 °C

3.1: bis-triphenylphosphine-palladium(II) chloride / toluene / 27 h / 110 °C

3.2: 16 h / 20 °C

4.1: 1-methyl-pyrrolidin-2-one / 1.5 h / 90 °C

5.1: potassium carbonate / 1-methyl-pyrrolidin-2-one / 65 h / 97 °C

6.1: water; sodium nitrite; acetic acid / 0.75 h / 60 °C

6.2: 0 °C / pH 7

7.1: trichlorophosphate / 5 h / 80 °C

7.2: 20 °C / pH 11

8.1: isopropyl alcohol / 70 °C

8.2: 48 h / 70 °C

9.1: triethylamine / dichloromethane / 20 °C

With N-iodo-succinimide; water; sodium hydrogencarbonate; potassium carbonate; acetic acid; triethylamine; sodium nitrite; trichlorophosphate; bis-triphenylphosphine-palladium(II) chloride; In 1-methyl-pyrrolidin-2-one; ethanol; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol; toluene;

Reference yield:

: 34658-67-8
2-(3-nitrophenyl)imidazo[1,2-a]pyridine

: 1301141-72-9
C₂₉H₂₅N₇O₄

Guidance literature:: Multi-step reaction with 8 steps

1.1: N-iodo-succinimide / N,N-dimethyl-formamide / 4 h / 20 °C

2.1: bis-triphenylphosphine-palladium(II) chloride / toluene / 27 h / 110 °C

2.2: 16 h / 20 °C

3.1: 1-methyl-pyrrolidin-2-one / 1.5 h / 90 °C

4.1: potassium carbonate / 1-methyl-pyrrolidin-2-one / 65 h / 97 °C

5.1: water; sodium nitrite; acetic acid / 0.75 h / 60 °C

5.2: 0 °C / pH 7

6.1: trichlorophosphate / 5 h / 80 °C

6.2: 20 °C / pH 11

7.1: isopropyl alcohol / 70 °C

7.2: 48 h / 70 °C

8.1: triethylamine / dichloromethane / 20 °C

With N-iodo-succinimide; water; potassium carbonate; acetic acid; triethylamine; sodium nitrite; trichlorophosphate; bis-triphenylphosphine-palladium(II) chloride; In 1-methyl-pyrrolidin-2-one; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol; toluene;