Water → HCID 19800237, compound

HRID 2248409Notes

Reaction equation

HRID 2248409 reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]2[C:10]([CH:18]([CH3:20])[CH3:19])=[CH:11][N:12]3[C:17]=2[CH:16]=[CH:15][CH:14]=[CH:13]3)=[CH:4][CH:3]=1.[C:21](=[O:24])([O-:23])[O-].[K+].[K+].Cl[CH:28]([N:31]([CH2:36][CH2:37][CH2:38][CH3:39])[CH2:32][CH2:33][CH2:34][CH3:35])[CH2:29][CH3:30].[OH2:40]>CS(C)=O>[C:2]([OH:1])(=[O:40])[C:21]([OH:23])=[O:24].[CH2:36]([N:31]([CH2:32][CH2:33][CH2:34][CH3:35])[CH2:28][CH2:29][CH2:30][O:1][C:2]1[CH:3]=[CH:4][C:5]([S:8][C:9]2[C:10]([CH:18]([CH3:20])[CH3:19])=[CH:11][N:12]3[C:17]=2[CH:16]=[CH:15][CH:14]=[CH:13]3)=[CH:6][CH:7]=1)[CH2:37][CH2:38][CH3:39]

Participants

6

Procedure

Into a solution of 0.01 mol of 1-[(4-hydroxyphenyl)thio]-2-isopropylindolizine in 80 ml of dimethylsulphoxide, there were added 5 g of anhydrous potassium carbonate and 0.015 mol of 1-chloro-di-n-butylamino-propane. The reaction medium was maintained under stirring for 24 hours and then poured into 500 ml of water. The solution was extracted with diethyl ether and the organic phase was washed with water, dried on sodium sulphate, filtered and evaporated to dryness to obtain the desired product in basic form. This crude compound was dissolved in dry diethyl ether and a solution of oxalic acid in diethyl ether was added.

Workup

  1. temperatureThe reaction medium was maintained
  2. extractionThe solution was extracted with diethyl ether
  3. washthe organic phase was washed with water
  4. customdried on sodium sulphate
  5. filtrationfiltered
  6. customevaporated to dryness

Sources & evidence

ORD record
ord-4bf197822fda446f9b112929bf5f4c78
Source dataset
uspto-grants-1991_08
Patent number
US05039700

Reaction notes

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