Basic information Safety Supplier Related

5-CHLOROACETYLOXINDOLE

Basic information Safety Supplier Related

5-CHLOROACETYLOXINDOLE Basic information

Product Name:
5-CHLOROACETYLOXINDOLE
Synonyms:
  • 2H-Indol-2-one, 5-(chloroacetyl)-1,3-dihydro- (9CI)
  • 5-(Chloroacetyl)-1,3-dihydro-2H-indol-2-one 98%
  • 1H-indol-5-yl 2-chloroacetate
  • 2H-Indol-2-one,5-(2-chloroacetyl)-1,3-dihydro-
  • 5-(2-chloroacetyl)indolin-2-one
  • 5-CHLOROACETYLOXINDOLE
  • (5-CHLOROACETYL)-1,3-DIHYDRO-2H-INDOL-2-ONE
  • 5-Chloroacetyl-2-indolinone
CAS:
65435-04-3
MF:
C10H8ClNO2
MW:
209.63
Product Categories:
  • ACETYLHALIDE
  • blocks
  • IndolesOxindoles
Mol File:
65435-04-3.mol
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5-CHLOROACETYLOXINDOLE Chemical Properties

Melting point:
228-232°C
Boiling point:
460.8±45.0 °C(Predicted)
Density 
1.361±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
slightly sol. in Dimethylformamide
form 
powder to crystal
pka
13.29±0.20(Predicted)
color 
White to Light yellow to Light orange
CAS DataBase Reference
65435-04-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
Hazard Note 
Irritant
HS Code 
2933790090
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5-CHLOROACETYLOXINDOLE Usage And Synthesis

Uses

5-(Chloroacetyl)oxindole is an intermediate used to prepare [(dihydrooxoindolylidene)methyl]pyrrolepropanoic acid and pyrido[2,3-d]pyrimidine as tyrosine kinase inhibitors.

Synthesis

59-48-3

79-04-9

65435-04-3

Under ice bath conditions, 5-carboxy-2-hydroxyindole (6.7 g) was slowly added to a stirred suspension of 30 mL of dichloroethane containing 23 g of aluminum chloride. Subsequently, chloroacetyl chloride (11.3 g) was added slowly and hydrogen chloride gas was released during the reaction. The reaction mixture was stirred for 10 minutes before being warmed to 40 to 50°C and maintained for 1.5 hours. The progress of the reaction was monitored by thin layer chromatography (Spreader: ethyl acetate, Stationary phase: silica gel) to confirm the complete consumption of the starting material. Upon completion of the reaction, the mixture was cooled to room temperature and carefully poured into ice water. The resulting precipitate was collected by vacuum filtration, washed well with water and dried under vacuum to give 10.3 g (98% yield) of the target product 5-chloroacetyl-2-hydroxyindole as an off-white solid.

References

[1] Journal of Medicinal Chemistry, 1991, vol. 34, # 6, p. 1860 - 1866
[2] Journal of Medicinal Chemistry, 1999, vol. 42, # 25, p. 5120 - 5130
[3] Patent: US6878733, 2005, B1. Location in patent: Page/Page column 172; 219
[4] Patent: US6350754, 2002, B2. Location in patent: Page column 23-24
[5] Journal of Heterocyclic Chemistry, 1991, vol. 28, # 6, p. 1525 - 1532

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