Diethyl Ether → HCID 46736522, compound
Reaction equation
[CH3:1][CH:2]1[CH2:7][CH2:6][CH2:5][NH:4][CH2:3]1.C(N(C(C)C)CC)(C)C.[ClH:17].[N:18]1(C(=N)N)[CH:22]=[N:21]C=N1.CCOCC>CN(C)C=O>[ClH:17].[CH3:1][CH:2]1[CH2:7][CH2:6][CH2:5][N:4]([C:22](=[NH:18])[NH2:21])[CH2:3]1Participants
Procedure
A mixture of 3-methylpiperidine (2.347 ml, 20 mmol), diisopropylethylamine (3.49 ml, 20.00 mmol) and 1H-1,2,4-triazole-1-carboximidamide hydrochloride (2.444 g, 22.00 mmol) in N,N-dimethylformamide (10 ml) was stirred at room temperature overnight. Ether (50 ml) was added to the reaction mixture and the mixture was stirred at room temperature for 10 minutes. The ether layer was separated and DMF layer was stirred with ether (50 ml) at 5° C. (ice water bath) for 10 minutes and the ether layer was separated from the residue. Ether (20 ml) was added to the residue and the mixture was stirred at 5° C. The resulting solid was triturated with ether, collected, washed with ether and dried to give the title compound as a colourless solid (2.95 g, 83%). LC/MS [M+H]+=142.
Workup
- stirringthe mixture was stirred at room temperature for 10 minutes
- customThe ether layer was separated
- stirringDMF layer was stirred with ether (50 ml) at 5° C. (ice water bath) for 10 minutes
- customthe ether layer was separated from the residue
- additionEther (20 ml) was added to the residue
- stirringthe mixture was stirred at 5° C
- customThe resulting solid was triturated with ether
- customcollected
- washwashed with ether
- customdried
Sources & evidence
- ORD record
- ord-c158fdf20f5348ff97621482ae302e35
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09133178B2
Reaction notes
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