C₂₄H₂₀ClN₅O

Base Information

Chemical Name:C₂₄H₂₀ClN₅O
CAS No.:1420623-06-8
Molecular Formula:C₂₄H₂₀ClN₅O
Molecular Weight:429.909
Hs Code.:

C<sub>24</sub>H<sub>20</sub>ClN<sub>5</sub>O

Synonyms:C₂₄H₂₀ClN₅O

Suppliers and Price of C₂₄H₂₀ClN₅O

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of C₂₄H₂₀ClN₅O

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₄H₂₀ClN₅O

There total 9 articles about C₂₄H₂₀ClN₅O 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: 87.2%

: 1350643-72-9
(S)-3-(1-aminoethyl)-8-chloro-2-phenylisoquinoline-1(2H)-one

: 154578-27-5
imidazo[1,2-b]pyridazine-3-carbaldehyde

: 1420623-06-8
C₂₄H₂₀ClN₅O

Guidance literature:: (S)-3-(1-aminoethyl)-8-chloro-2-phenylisoquinoline-1(2H)-one; imidazo[1,2-b]pyridazine-3-carbaldehyde; With sodium tris(acetoxy)borohydride; acetic acid; In dichloromethane; at 20 ℃; for 2h;

With water; In dichloromethane;

Reference yield:

: 21327-86-6
2-chloro-6-methylbenzoic acid

: 1420623-06-8
C₂₄H₂₀ClN₅O

Guidance literature:: Multi-step reaction with 3 steps

1.1: N,N-dimethyl-formamide; oxalyl dichloride / dichloromethane / 2.08 h / 20 °C

1.2: 2 h / 20 °C

2.1: n-butyllithium / tetrahydrofuran; hexane / 1 h / -30 - -10 °C / Inert atmosphere

2.2: 2 h / -50 - -10 °C / Inert atmosphere

3.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 2 h / 20 °C

With n-butyllithium; oxalyl dichloride; sodium tris(acetoxy)borohydride; acetic acid; N,N-dimethyl-formamide; In tetrahydrofuran; hexane; dichloromethane;

Reference yield:

: 1386861-47-7
tert-butyl (S)-(4-(3-chloro-2-(phenylcarbamoyl)phenyl)-3-oxobutane-2-yl)carbamate

: 1420623-06-8
C₂₄H₂₀ClN₅O

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / water; isopropyl alcohol / 3 h / 65 °C

2: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 2 h / 20 °C

With hydrogenchloride; sodium tris(acetoxy)borohydride; acetic acid; In dichloromethane; water; isopropyl alcohol;