Indoline → HCID 12524226, compound

HRID 557230Notes

Reaction equation

HRID 557230 reaction equation
FC(F)(F)S(OS(C(F)(F)F)(=O)=O)(=O)=O.CN(C)[C:18](=[O:21])[CH:19]=[CH2:20].[NH:23]1[C:31]2[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=2)[CH2:25][CH2:24]1>ClC(Cl)C>[CH2:25]1[C:26]2=[C:31]3[C:30](=[CH:29][CH:28]=[CH:27]2)[C:18](=[O:21])[CH2:19][CH2:20][N:23]3[CH2:24]1

Participants

5

Procedure

Add trifluoromethanesulfonic anhydride (10.5 mL, 63 mmol) in dichloroethane (30 mL) to N,N-dimethylacrylamide (6.4 mL, 63 mmol) in dichloroethane (100 mL) at 0° C. dropwise with vigorous stirring over 5 minutes. Add indoline (5.6 mL, 50 mmol) in dichloroethane (30 mL) dropwise over 5 minutes. Remove from cooling bath and heat at reflux for 3.5 hours. Cool to room temperature. Dilute with diethyl ether (600 mL). Wash with aqueous potassium carbonate (400 mL), dilute aqueous sodium bicarbonate (2×300 mL) and saturated aqueous sodium chloride (300 mL). Dry over sodium sulfate and concentrate under reduced pressure. Subject the residue to chromatography (pre-packed silica gel), eluting with 19:1 dichloromethane/ethyl acetate to provide the desired compound (2.65 g, 31%).

Workup

  1. customRemove
  2. temperaturefrom cooling bath
  3. temperatureheat
  4. temperatureat reflux for 3.5 hours
  5. additionDilute with diethyl ether (600 mL)
  6. washWash with aqueous potassium carbonate (400 mL), dilute aqueous sodium bicarbonate (2×300 mL) and saturated aqueous sodium chloride (300 mL)
  7. dry with materialDry over sodium sulfate
  8. concentrationconcentrate under reduced pressure
  9. washeluting with 19:1 dichloromethane/ethyl acetate

Sources & evidence

ORD record
ord-4eb7b18b5e2f4d7fa6105e934bed2185
Source dataset
uspto-grants-2011_11
Patent number
US08058425B2

Reaction notes

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