C₂₄H₁₉ClN₄O

Base Information

Chemical Name:C₂₄H₁₉ClN₄O
CAS No.:1414781-97-7
Molecular Formula:C₂₄H₁₉ClN₄O
Molecular Weight:414.894
Hs Code.:

C<sub>24</sub>H<sub>19</sub>ClN<sub>4</sub>O

Synonyms:C₂₄H₁₉ClN₄O

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Chemical Property of C₂₄H₁₉ClN₄O

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Technology Process of C₂₄H₁₉ClN₄O

There total 5 articles about C₂₄H₁₉ClN₄O 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: 65.0%

: 1414781-96-6
C₂₄H₁₇ClN₄O

: 1414781-97-7
C₂₄H₁₉ClN₄O

Guidance literature:: C₂₄H₁₇ClN₄O; With oxalyl dichloride; In chloroform; at 0 ℃; for 1h; Reflux;

With sodium cyanoborohydride; In tetrahydrofuran; at 0 - 25 ℃; for 24h;
DOI:10.1021/jm300831b

Reference yield:

: 100-46-9
benzylamine

: 1414781-97-7
C₂₄H₁₉ClN₄O

Guidance literature:: Multi-step reaction with 4 steps

1.1: toluene-4-sulfonic acid / 0.5 h / 150 °C / Microwave irradiation

2.1: tin(II) chloride dihdyrate / ethyl acetate / 2 h / Reflux

3.1: ethanol / 48 h / Reflux

4.1: oxalyl dichloride / chloroform / 1 h / 0 °C / Reflux

4.2: 24 h / 0 - 25 °C

With oxalyl dichloride; tin(II) chloride dihdyrate; toluene-4-sulfonic acid; In ethanol; chloroform; ethyl acetate;
DOI:10.1021/jm300831b

Reference yield:

: 619-17-0
4-Nitroanthranilic acid

: 1414781-97-7
C₂₄H₁₉ClN₄O

Guidance literature:: Multi-step reaction with 4 steps

1.1: toluene-4-sulfonic acid / 0.5 h / 150 °C / Microwave irradiation

2.1: tin(II) chloride dihdyrate / ethyl acetate / 2 h / Reflux

3.1: ethanol / 48 h / Reflux

4.1: oxalyl dichloride / chloroform / 1 h / 0 °C / Reflux

4.2: 24 h / 0 - 25 °C

With oxalyl dichloride; tin(II) chloride dihdyrate; toluene-4-sulfonic acid; In ethanol; chloroform; ethyl acetate;
DOI:10.1021/jm300831b