C₂₃H₂₆Cl₂N₆O₄S

Base Information

Chemical Name:C₂₃H₂₆Cl₂N₆O₄S
CAS No.:1353628-94-0
Molecular Formula:C₂₃H₂₆Cl₂N₆O₄S
Molecular Weight:553.469
Hs Code.:

C<sub>23</sub>H<sub>26</sub>Cl<sub>2</sub>N<sub>6</sub>O<sub>4</sub>S

Synonyms:C₂₃H₂₆Cl₂N₆O₄S

Suppliers and Price of C₂₃H₂₆Cl₂N₆O₄S

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 C₂₃H₂₆Cl₂N₆O₄S

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₃H₂₆Cl₂N₆O₄S

There total 8 articles about C₂₃H₂₆Cl₂N₆O₄S 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:

: 124668-46-8
3-hydroxyl-3-methylazetidine hydrochloride

: 1353628-61-1
(S)-N-(4-chloro-2-(2-(5,7-dichloropyrazolo[1,5-a]pyrimidin-2-yl)piperidine-1-carbonyl)phenyl)methanesulfonamide

: 1353628-94-0
C₂₃H₂₆Cl₂N₆O₄S

Guidance literature:: With sodium hydrogencarbonate; In tetrahydrofuran; at 20 ℃; for 36h;

Reference yield:

: 26250-84-0
(S)-(-)-1-(tert-butoxycarbonyl)-2-piperidinecarboxylic acid

: 1353628-94-0
C₂₃H₂₆Cl₂N₆O₄S

Guidance literature:: Multi-step reaction with 7 steps

1.1: caesium carbonate / N,N-dimethyl-formamide / 4 h

2.1: sodium bis(trimethylsilyl)amide / tetrahydrofuran; hexanes / -78 - -40 °C

2.2: -78 - -40 °C

2.3: -78 - 20 °C

3.1: hydrazinium monoacetate / ethanol / 16 h / 20 °C

4.1: sodium methylate / methanol / 5 h / 78 °C

5.1: trichlorophosphate / 3 h / 100 °C

6.1: oxalyl dichloride / dichloromethane; N,N-dimethyl-formamide / 3 h / 20 °C

6.2: 0.67 h / 20 °C / Cooling with ice

7.1: sodium hydrogencarbonate / tetrahydrofuran / 36 h / 20 °C

With oxalyl dichloride; sodium bis(trimethylsilyl)amide; sodium methylate; hydrazinium monoacetate; sodium hydrogencarbonate; caesium carbonate; trichlorophosphate; In tetrahydrofuran; methanol; hexanes; ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 203056-27-3
tert-butyl (2S)-2-{[methoxy(methyl)amino]-carbonyl}piperidine-1-carboxylate

: 1353628-94-0
C₂₃H₂₆Cl₂N₆O₄S

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium bis(trimethylsilyl)amide / tetrahydrofuran / 0.42 h / -78 - -20 °C / Inert atmosphere

1.2: 3.08 h / -78 - -45 °C

1.3: -78 - 20 °C

2.1: hydrazinium monoacetate / ethanol / 16 h / 20 °C

3.1: sodium methylate / methanol / 5 h / 78 °C

4.1: trichlorophosphate / 3 h / 100 °C

5.1: oxalyl dichloride / dichloromethane; N,N-dimethyl-formamide / 3 h / 20 °C

5.2: 0.67 h / 20 °C / Cooling with ice

6.1: sodium hydrogencarbonate / tetrahydrofuran / 36 h / 20 °C

With oxalyl dichloride; sodium bis(trimethylsilyl)amide; sodium methylate; hydrazinium monoacetate; sodium hydrogencarbonate; trichlorophosphate; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;