139122-20-6

  • Product Name:4-(2'-Hydroxyethyl) Oxindole P-Toluenesulfonate
  • Molecular Formula:C17H17NO4S
  • Purity:99%
  • Molecular Weight:331.392
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Product Details;

CasNo: 139122-20-6

Molecular Formula: C17H17NO4S

Factory supply 4-(2'-Hydroxyethyl) Oxindole P-Toluenesulfonate 139122-20-6 with sufficient production capacity

  • Molecular Formula:C17H17NO4S
  • Molecular Weight:331.392
  • Boiling Point:561.181 °C at 760 mmHg 
  • PKA:14.02±0.20(Predicted) 
  • Flash Point:293.192 °C 
  • PSA:80.85000 
  • Density:1.312 g/cm3 
  • LogP:3.65640 

139122-20-6 Relevant articles

Design, synthesis, and biological evaluation of structurally constrained hybrid analogues containing ropinirole moiety as a novel class of potent and selective dopamine D3 receptor ligands

Zhou, Benhua,Hong, Kwon Ho,Ji, Min,Cai, Jin

, p. 1597 - 1609 (2018/07/31)

Two series of hybrid analogues were desi...

Method for preparing ropinirole hydrochloride

-

Paragraph 0062; 0063; 0064, (2018/09/12)

The invention belongs to the technical f...

Indoline-2-ketone D3 receptor ligand and preparation method and application thereof

-

Paragraph 0068; 0069, (2016/10/08)

The invention discloses an indoline-2-ke...

Improved preparation method for ropinirole hydrochloride

-

Paragraph 0051; 0052, (2016/10/09)

The invention discloses an improved prep...

139122-20-6 Process route

2-(2-bromoethyl)benzaldehyde
22901-09-3

2-(2-bromoethyl)benzaldehyde

2-(2-oxo-2,3-dihydro-1H-indol-4-yl)ethyl-4-methylbenzene-1-sulfonate
139122-20-6

2-(2-oxo-2,3-dihydro-1H-indol-4-yl)ethyl-4-methylbenzene-1-sulfonate

Conditions
Conditions Yield
Multi-step reaction with 6 steps
1: 80 percent / MeONa / methanol / 1 h / 0 °C
2: 53 percent / AcCl, FeCl3 / CH2Cl2 / 3 h / 0 - 5 °C
3: 95 percent / aq. NaH2PO2 / 10percent Pd-C / ethyl acetate / 0.58 h / Heating
4: 89 percent / ethanol; H2O / 24 h / Heating
5: 70 percent / aq. HCl / 2.5 h / Heating
6: 87 percent / pyridine / CH2Cl2 / 4 h / 5 - 10 °C
With pyridine; hydrogenchloride; sodium hypophosphite; sodium methylate; iron(III) chloride; acetyl chloride; palladium on activated charcoal; In methanol; ethanol; dichloromethane; water; ethyl acetate;
 
p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

4-(2'-hydroxyethyl)-1,3-dihydro-2H-indol-2-one
139122-19-3

4-(2'-hydroxyethyl)-1,3-dihydro-2H-indol-2-one

2-(2-oxo-2,3-dihydro-1H-indol-4-yl)ethyl-4-methylbenzene-1-sulfonate
139122-20-6

2-(2-oxo-2,3-dihydro-1H-indol-4-yl)ethyl-4-methylbenzene-1-sulfonate

Conditions
Conditions Yield
With pyridine; In dichloromethane; at 5 - 10 ℃; for 4h;
87%
With pyridine; Large scale;
87%
With pyridine; In dichloromethane; at 5 - 10 ℃; for 3h;
86%
In pyridine; dichloromethane; at 5 - 10 ℃; for 3h;
86%
With pyridine; In dichloromethane; at 5 - 10 ℃; for 2h;
86%
With pyridine; In dichloromethane; at 5 - 10 ℃; for 4.5h;
80%
With pyridine; In dichloromethane; at 5 - 10 ℃; for 4.5h;
80%
With pyridine; In dichloromethane; at 0 - 20 ℃;
 
With pyridine; at 20 ℃; for 2h;
 

139122-20-6 Upstream products

  • 98-59-9
    98-59-9

    p-toluenesulfonyl chloride

  • 139122-19-3
    139122-19-3

    4-(2'-hydroxyethyl)-1,3-dihydro-2H-indol-2-one

  • 493-05-0
    493-05-0

    isochromane

  • 22901-09-3
    22901-09-3

    2-(2-bromoethyl)benzaldehyde

139122-20-6 Downstream products

  • 91374-20-8
    91374-20-8

    ropinirole hydrochloride

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