Hydrochloric Acid → HCID 19854389, compound
Reaction equation
[ClH:1].C(OC([NH:9][CH2:10][CH2:11][S:12][C:13]1[CH:14]=[CH:15][C:16]2[N:17]([CH:19]=[CH:20][N:21]=2)[N:18]=1)=O)(C)(C)C>>[ClH:1].[ClH:1].[NH2:9][CH2:10][CH2:11][S:12][C:13]1[CH:14]=[CH:15][C:16]2[N:17]([CH:19]=[CH:20][N:21]=2)[N:18]=1Participants
3
Procedure
To 100 ml of 3N-hydrochloric acid is added 5.89 g of 6-(2-tert-butoxycarbonylaminoethylthio)imidazo[1,2-b]pyridazine and the mixture is refluxed with stirring for 20 minutes. The solvent is distilled off under reduced pressure and the residue is diluted with 50 ml of toluene and concentrated again under reduced pressure. To the residue is added ether and the resulting powers are collected by filtration and washed with ether, ethanol and ether in the order mentioned to give 5.26 g of 6-(2-aminoethylthio)imidazo[ 1,2-b]pyridazine dihydrochloride as colorless powders.
Workup
- temperaturethe mixture is refluxed
- distillationThe solvent is distilled off under reduced pressure
- additionthe residue is diluted with 50 ml of toluene
- concentrationconcentrated again under reduced pressure
- additionTo the residue is added ether
- filtrationthe resulting powers are collected by filtration
- washwashed with ether, ethanol and ether in the order
Sources & evidence
- ORD record
- ord-470ae79806e74e7380760593fe5586ee
- Source dataset
- uspto-grants-1990_05
- Patent number
- US04921851
Reaction notes
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