Sodium Iodide → [4-acetylamino-3-(4-chlorophenylsulfanyl)-2-methyl-1H-indol-1-yl]acetic acid ethyl ester

HRID 1516982Notes

Reaction equation

HRID 1516982 reaction equation
[I-].[Na+].[C:3](OC(=O)C)(=[O:5])[CH3:4].[Cl:10][C:11]1[CH:16]=[CH:15][C:14]([S:17][C:18]2[C:26]3[C:25](=[N:27]O)[CH2:24][CH2:23][CH2:22][C:21]=3[N:20]([CH2:29][C:30]([O:32][CH2:33][CH3:34])=[O:31])[C:19]=2[CH3:35])=[CH:13][CH:12]=1.S([O-])([O-])(=O)=S.[Na+].[Na+]>C1(C)C(C)=CC=CC=1.C(O)(=O)C.O>[C:3]([NH:27][C:25]1[CH:24]=[CH:23][CH:22]=[C:21]2[C:26]=1[C:18]([S:17][C:14]1[CH:15]=[CH:16][C:11]([Cl:10])=[CH:12][CH:13]=1)=[C:19]([CH3:35])[N:20]2[CH2:29][C:30]([O:32][CH2:33][CH3:34])=[O:31])(=[O:5])[CH3:4]

Participants

8

Reactant 4

HCID 5238Sodium IodideHCID 7918Acetic Anhydride2×HCID 24477Sodium ThiosulfateHCID 76689533HCID 76689533, compound

Product 1

HCID 11546184[4-acetylamino-3-(4-chlorophenylsulfanyl)-2-methyl-1H-indol-1-yl]acetic acid ethyl esterYield 81%

Reagents, catalysts & solvents 3

HCID 176Acetic AcidSolvent2×HCID 962WaterSolventHCID 7237O-XyleneSolvent2×

Conditions

Temperature
102.5 °C

Procedure

A mixture of sodium iodide (0.0625 mol equiv) in xylene (1.99 rel vol), acetic acid (0.27 rel vol) and acetic anhydride (1.27 mole equiv) was heated to 102.5° C. in vessel 1 with stirring. In vessel 2, acetic anhydride (1.27 mole equiv) was added to a stirred slurry of ethyl [3-(4-chlorophenylsulfanyl)-4-(hydroxyimino)-2-methyl-4,5,6,7-tetrahydro-1H-indol-1-yl]acetate (1 mole equiv, limiting reagent) in xylene (2.24 rel vol) and acetic acid (0.27 rel vol) at 22° C. After stirring at this temperature for 30 mins, this mixture was added to the contents of reaction vessel 1 over 50 mins maintaining the temperature at 102.5° C. The reaction was held at this temperature for a further 2.5 h. The reaction was cooled to 60° C. and sodium thiosulfate (0.05 mole equiv) and water (0.5 rel vol) were added. After mixing, and allowing the layers to separate, the lower aqueous layer was discarded then the organic layer was distilled under vacuum, removing 1.8 rel vol distillate. The temperature was adjusted to 95° C. and the product precipitated by the addition of heptanes (3 rel vol). The suspension was cooled to 20° C. over 1 h then the solid product was collected by filtration, washed with ethanol (2 rel vol) and dried in vacuo at 40° C. to afford crude ethyl [4-acetylamino-3-(4-chlorophenylsulfanyl)-2-methyl-1H-indol-1-yl]acetate as a solid; 81% yield; purity by UHPLC 98.3 area %.

Workup

  1. stirringAfter stirring at this temperature for 30 mins
  2. additionthis mixture was added to the contents of reaction vessel 1 over 50 mins
  3. temperaturemaintaining the temperature at 102.5° C
  4. temperatureThe reaction was cooled to 60° C.
  5. additionAfter mixing
  6. customto separate
  7. distillationthe organic layer was distilled under vacuum
  8. customremoving 1.8 rel vol distillate
  9. customwas adjusted to 95° C.
  10. customthe product precipitated by the addition of heptanes (3 rel vol)
  11. temperatureThe suspension was cooled to 20° C. over 1 h
  12. filtrationthe solid product was collected by filtration
  13. washwashed with ethanol (2 rel vol)
  14. customdried in vacuo at 40° C.

Sources & evidence

ORD record
ord-653de496b3dd493892dc045563382348
Source dataset
uspto-grants-2012_07
Patent number
US08227622B2

Reaction notes

Loading…