1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → HCID 17842642, compound
Reaction equation
O.ON1C2C=CC=C[C:6]=2N=N1.Cl.CN(C)CCCN=C=NCC.[N:24]1[CH:29]=[CH:28][C:27]([C:30]2[S:34][C:33]([C:35]([O-:37])=[O:36])=[N:32][CH:31]=2)=[CH:26][CH:25]=1.[Li+]>CO>[N:24]1[CH:29]=[CH:28][C:27]([C:30]2[S:34][C:33]([C:35]([O:37][CH3:6])=[O:36])=[N:32][CH:31]=2)=[CH:26][CH:25]=1Participants
Procedure
1-Hydroxybenzotriazole monohydrate (805 mg) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.71 g) were added to a solution of lithium 5-(4-pyridyl)thiazole-2-carboxylate (632 mg) in methanol (5.0 ml) at room temperature. After stirring for 4 days, the reaction mixture was concentrated under reduced pressure, and dichloromethane (20 ml), a saturated aqueous solution (100 ml) of sodium hydrogencarbonate and water (100 ml) were added to the residue to separate an organic layer. The water layer was then extracted with dichloromethane (2×20 ml). After the resultant organic layers were combined and dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was then purified by column chromatography on silica gel (dichloromethane:acetone=5:1→2:1) to obtain the title compound (353 mg) as a colorless solid.
Workup
- concentrationthe reaction mixture was concentrated under reduced pressure, and dichloromethane (20 ml)
- additiona saturated aqueous solution (100 ml) of sodium hydrogencarbonate and water (100 ml) were added to the residue
- customto separate an organic layer
- extractionThe water layer was then extracted with dichloromethane (2×20 ml)
- dry with materialdried over anhydrous sodium sulfate
- distillationthe solvent was distilled off under reduced pressure
- customThe residue was then purified by column chromatography on silica gel (dichloromethane:acetone=5:1→2:1)
Sources & evidence
- ORD record
- ord-2798ffb9953e4127b3f8eafb5c32e643
- Source dataset
- uspto-grants-2011_05
- Patent number
- US07935824B2
Reaction notes
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