Potassium Carbonate → HCID 178424873, compound

HRID 1956535Notes

Reaction equation

HRID 1956535 reaction equation
[C:1]([O:5][C:6](=[O:29])[NH:7][CH2:8][CH2:9][C:10]1[C:18]2[C:13](=[CH:14][CH:15]=[C:16]([C:19]#[N:20])[CH:17]=2)[NH:12][C:11]=1[C:21]1[CH:26]=[C:25]([CH3:27])[CH:24]=[C:23]([CH3:28])[CH:22]=1)([CH3:4])([CH3:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+].Cl.[NH2:37][OH:38]>C(O)C>[C:1]([O:5][C:6](=[O:29])[NH:7][CH2:8][CH2:9][C:10]1[C:18]2[C:13](=[CH:14][CH:15]=[C:16]([C:19](=[NH:20])[NH:37][OH:38])[CH:17]=2)[NH:12][C:11]=1[C:21]1[CH:26]=[C:25]([CH3:27])[CH:24]=[C:23]([CH3:28])[CH:22]=1)([CH3:4])([CH3:3])[CH3:2]

Participants

5

Procedure

A solution of {2-[5-cyano-2-(3,5-dimethylphenyl)-1H-indol-3-yl]ethyl}carbamic acid tert-butyl ester (300 mg in 5 mL ethanol) was added to a suspension of 725 mg potassium carbonate and 273 mg hydroxylamine hydrochloride in 7 mL ethanol and the whole heated to reflux on an oil bath. After 21 hours, the mixture was cooled to room temperature and filtered to remove solids. The filtrate was concentrated in vacuo then partitioned between ethyl acetate and water. The organic portion was washed with water, dried over sodium sulfate and the concentrate purified by flash chromatography on silica gel (methylene chloride:methanol, 92:8) to give the title compound (105 mg).

Workup

  1. temperaturethe whole heated
  2. temperatureto reflux on an oil bath
  3. filtrationfiltered
  4. customto remove solids
  5. concentrationThe filtrate was concentrated in vacuo
  6. customthen partitioned between ethyl acetate and water
  7. washThe organic portion was washed with water
  8. dry with materialdried over sodium sulfate
  9. customthe concentrate purified by flash chromatography on silica gel (methylene chloride:methanol, 92:8)

Sources & evidence

ORD record
ord-d9d0e1e3de8a4fd1a9eb756cdb252b93
Source dataset
uspto-grants-1998_07
Patent number
US05780437

Reaction notes

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