5-cyclopropyl-2-[4-(4-fluorophenoxy)phenyl]-6-[(2-hydroxyethyl)(methylsulfonyl)amino]-N-methyl-2H-indazole-3-carboxamide

Base Information

Chemical Name:5-cyclopropyl-2-[4-(4-fluorophenoxy)phenyl]-6-[(2-hydroxyethyl)(methylsulfonyl)amino]-N-methyl-2H-indazole-3-carboxamide
CAS No.:1373839-75-8
Molecular Formula:C₂₇H₂₇FN₄O₅S
Molecular Weight:538.6
Hs Code.:

Synonyms:5-cyclopropyl-2-[4-(4-fluorophenoxy)phenyl]-6-[(2-hydroxyethyl)(methylsulfonyl)amino]-N-methyl-2H-indazole-3-carboxamide

Suppliers and Price of 5-cyclopropyl-2-[4-(4-fluorophenoxy)phenyl]-6-[(2-hydroxyethyl)(methylsulfonyl)amino]-N-methyl-2H-indazole-3-carboxamide

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 5-cyclopropyl-2-[4-(4-fluorophenoxy)phenyl]-6-[(2-hydroxyethyl)(methylsulfonyl)amino]-N-methyl-2H-indazole-3-carboxamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 5-cyclopropyl-2-[4-(4-fluorophenoxy)phenyl]-6-[(2-hydroxyethyl)(methylsulfonyl)amino]-N-methyl-2H-indazole-3-carboxamide

There total 10 articles about 5-cyclopropyl-2-[4-(4-fluorophenoxy)phenyl]-6-[(2-hydroxyethyl)(methylsulfonyl)amino]-N-methyl-2H-indazole-3-carboxamide 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: 34.0%

: 1373844-69-9
5-cyclopropyl-2-[4-(4-fluorophenoxy)phenyl]-N-methyl-6-[(methylsulfonyl)amino]-2H-indazole-3-carboxamide

: 540-51-2
2-bromoethanol

: 1373839-75-8
5-cyclopropyl-2-[4-(4-fluorophenoxy)phenyl]-6-[(2-hydroxyethyl)(methylsulfonyl)amino]-N-methyl-2H-indazole-3-carboxamide

Guidance literature:: With potassium carbonate; In acetonitrile; at 80 ℃; for 16h;

Reference yield:

: 3132-99-8
m-bromobenzoic aldehyde

: 1373839-75-8
5-cyclopropyl-2-[4-(4-fluorophenoxy)phenyl]-6-[(2-hydroxyethyl)(methylsulfonyl)amino]-N-methyl-2H-indazole-3-carboxamide

Guidance literature:: Multi-step reaction with 11 steps

1.1: nitric acid; sulfuric acid / 0.42 h / cooling with ice

2.1: nitric acid; sulfuric acid / 6 h / 50 °C / cooling with ice

3.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / toluene; water / 6 h / Inert atmosphere; Reflux

4.1: acetic acid / 60 °C

4.2: 0.08 h / 60 °C

5.1: phosphorus trichloride / chloroform / 1 h / 60 °C

6.1: sodium hydroxide; water / ethanol / 15 h / 90 °C

7.1: pyridine; trichlorophosphate / tetrahydrofuran / 1 h / 0 °C

8.1: water; ammonium chloride; iron / ethanol / 1.5 h / 80 °C

9.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 20 °C

10.1: potassium carbonate; copper / copper(l) iodide / pyridine / 16 h / 150 °C / Sealed tube

11.1: potassium carbonate / acetonitrile / 16 h / 80 °C

With pyridine; sulfuric acid; water; nitric acid; iron; copper; sodium carbonate; potassium carbonate; ammonium chloride; acetic acid; N-ethyl-N,N-diisopropylamine; sodium hydroxide; trichlorophosphate; phosphorus trichloride; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; pyridine; ethanol; dichloromethane; chloroform; water; toluene; acetonitrile; 3.1: Suzuki Coupling;

Reference yield:

: 20357-20-4
5-bromo-2-nitrobenzaldehyde

: 1373839-75-8
5-cyclopropyl-2-[4-(4-fluorophenoxy)phenyl]-6-[(2-hydroxyethyl)(methylsulfonyl)amino]-N-methyl-2H-indazole-3-carboxamide

Guidance literature:: Multi-step reaction with 10 steps

1.1: nitric acid; sulfuric acid / 6 h / 50 °C / cooling with ice

2.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / toluene; water / 6 h / Inert atmosphere; Reflux

3.1: acetic acid / 60 °C

3.2: 0.08 h / 60 °C

4.1: phosphorus trichloride / chloroform / 1 h / 60 °C

5.1: sodium hydroxide; water / ethanol / 15 h / 90 °C

6.1: pyridine; trichlorophosphate / tetrahydrofuran / 1 h / 0 °C

7.1: water; ammonium chloride; iron / ethanol / 1.5 h / 80 °C

8.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 20 °C

9.1: potassium carbonate; copper / copper(l) iodide / pyridine / 16 h / 150 °C / Sealed tube

10.1: potassium carbonate / acetonitrile / 16 h / 80 °C

With pyridine; sulfuric acid; water; nitric acid; iron; copper; sodium carbonate; potassium carbonate; ammonium chloride; acetic acid; N-ethyl-N,N-diisopropylamine; sodium hydroxide; trichlorophosphate; phosphorus trichloride; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; pyridine; ethanol; dichloromethane; chloroform; water; toluene; acetonitrile; 2.1: Suzuki Coupling;