C₂₄H₁₉F₄N₇O₅S

Base Information

Chemical Name:C₂₄H₁₉F₄N₇O₅S
CAS No.:1612242-58-6
Molecular Formula:C₂₄H₁₉F₄N₇O₅S
Molecular Weight:593.518
Hs Code.:

C<sub>24</sub>H<sub>19</sub>F<sub>4</sub>N<sub>7</sub>O<sub>5</sub>S

Synonyms:C₂₄H₁₉F₄N₇O₅S

Suppliers and Price of C₂₄H₁₉F₄N₇O₅S

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 C₂₄H₁₉F₄N₇O₅S

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₄H₁₉F₄N₇O₅S

There total 13 articles about C₂₄H₁₉F₄N₇O₅S 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:

: N-[(S)-2-amino-2-(3-fluoro-4-trifluoromethyl-phenyl)-ethyl]-N-methyl-4-nitro-benzenesulfonamide hydrochloride

: 1612242-44-0
4-hydroxy-pyrido[3,2-d]pyrimidine-8-carboxamide

: 1612242-58-6
C₂₄H₁₉F₄N₇O₅S

Guidance literature:: N-[(S)-2-amino-2-(3-fluoro-4-trifluoromethyl-phenyl)-ethyl]-N-methyl-4-nitro-benzenesulfonamide hydrochloride; 4-hydroxy-pyrido[3,2-d]pyrimidine-8-carboxamide; With N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; at 20 ℃; for 0.0833333h; Inert atmosphere;

With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; In dimethyl sulfoxide; at 40 ℃; for 12h;

Reference yield:

: 1612242-47-3
3-nitro-pyridine-2,4-dicarboxylic acid diethyl ester

: 1612242-58-6
C₂₄H₁₉F₄N₇O₅S

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogen; palladium 10% on activated carbon / 4 h / 20 °C

2.1: 96 h / 140 °C

3.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 0.08 h / 20 °C / Inert atmosphere

3.2: 12 h / 40 °C

With palladium 10% on activated carbon; hydrogen; N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide;

Reference yield:

: 21901-18-8
4-Methyl-3-nitro-2-pyridone

: 1612242-58-6
C₂₄H₁₉F₄N₇O₅S

Guidance literature:: Multi-step reaction with 8 steps

1.1: phosphorus(V) oxybromide / 1,2-dichloro-ethane / 12 h / 20 °C / Reflux

2.1: N,N-dimethyl-formamide / 13 h / 100 °C

3.1: sulfuric acid / water / 3 h / 70 °C

4.1: hydrogenchloride; ammonium chloride; iron / water; isopropyl alcohol / Reflux

5.1: 24 h / Reflux

6.1: sulfuric acid; potassium dichromate; Pyrimidin-2(1H)-one / water / 20 - 30 °C

7.1: 1,1'-carbonyldiimidazole / N,N-dimethyl-formamide / 70 °C

7.2: 70 °C

8.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 0.08 h / 20 °C / Inert atmosphere

8.2: 12 h / 40 °C

With Pyrimidin-2(1H)-one; hydrogenchloride; potassium dichromate; sulfuric acid; iron; ammonium chloride; N-ethyl-N,N-diisopropylamine; 1,1'-carbonyldiimidazole; phosphorus(V) oxybromide; In water; dimethyl sulfoxide; 1,2-dichloro-ethane; N,N-dimethyl-formamide; isopropyl alcohol;