C₂₆H₂₄ClN₇O₂

Base Information

Chemical Name:C₂₆H₂₄ClN₇O₂
CAS No.:1441309-01-8
Molecular Formula:C₂₆H₂₄ClN₇O₂
Molecular Weight:501.975
Hs Code.:

C<sub>26</sub>H<sub>24</sub>ClN<sub>7</sub>O<sub>2</sub>

Synonyms:C₂₆H₂₄ClN₇O₂

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Chemical Property of C₂₆H₂₄ClN₇O₂

Chemical Property:

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Technology Process of C₂₆H₂₄ClN₇O₂

There total 6 articles about C₂₆H₂₄ClN₇O₂ 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:

: 1420627-35-5
(S)-2-(1-aminoethyl)-5-chloro-3-phenylquinazoline-4(3H)-one

: 7306-68-5
6-chloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine

: 1441309-01-8
C₂₆H₂₄ClN₇O₂

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In isopropyl alcohol; at 80 ℃; for 36h; Inert atmosphere; Sealed tube;

Reference yield:

: 20829-96-3
5-chloro-1H-benzo[d][1,3]oxazine-2,4-dione

: 1441309-01-8
C₂₆H₂₄ClN₇O₂

Guidance literature:: Multi-step reaction with 5 steps

1.1: 1,4-dioxane / 4.5 h / 40 - 100 °C

2.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 1 h / -15 °C

2.2: 21 - 60 °C

3.1: triethylamine; chloro-trimethyl-silane / acetonitrile / 48 h / 90 °C / Inert atmosphere

4.1: trifluoroacetic acid / dichloromethane / 2 h / 21 °C

5.1: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 36 h / 80 °C / Inert atmosphere; Sealed tube

With 4-methyl-morpholine; chloro-trimethyl-silane; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; isobutyl chloroformate; In tetrahydrofuran; 1,4-dioxane; dichloromethane; isopropyl alcohol; acetonitrile;

Reference yield:

: 50460-70-3
2-amino-6-chloro-N-phenylbenzamide

: 1441309-01-8
C₂₆H₂₄ClN₇O₂

Guidance literature:: Multi-step reaction with 4 steps

1.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 1 h / -15 °C

1.2: 21 - 60 °C

2.1: triethylamine; chloro-trimethyl-silane / acetonitrile / 48 h / 90 °C / Inert atmosphere

3.1: trifluoroacetic acid / dichloromethane / 2 h / 21 °C

4.1: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 36 h / 80 °C / Inert atmosphere; Sealed tube

With 4-methyl-morpholine; chloro-trimethyl-silane; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; isobutyl chloroformate; In tetrahydrofuran; dichloromethane; isopropyl alcohol; acetonitrile;