Sodium Chloride → HCID 136383532, compound
Reaction equation
C[O-].[Na+].Cl.[NH2:5][C:6]([NH2:8])=N.[CH:9]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH2:12][CH2:11][C:10]=1[C:19]([O:21]CC)=O.[Cl-].[Na+].C[N:27](C)C=O>>[NH2:27][N:5]=[CH:6][NH:8][C:19]([C:10]1[CH2:11][CH2:12][C:13]2[C:18](=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:9]=1)=[O:21]Participants
Procedure
A mixture of sodium methoxide (5.34 g, 98.9 mmol), guanidine hydrochloride (9.45 g, 98.9 mmol) and N,N-dimethylformamide (60 ml) was stirred at room temperature for 1 hour. Then, a solution of ethyl 3,4-dihydronaphthalene-2-carboxylate (2.00 g, 9.89 mmol) in N,N-dimethylformamide (20 ml) was added dropwise to the reaction mixture. The resulting mixture was stirred at room temperature for 7 hours and then allowed to stand overnight at room temperature. This reaction mixture was poured into a cold aqueous sodium chloride solution and extracted twice with ethyl acetate, and the extract solution was washed twice with a 5% aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain crude N-(aminoiminomethyl)-3,4-dihydronaphthalene-2-carboxamide. This compound was dissolved in isopropyl alcohol, followed by adding thereto excess methanesulfonic acid, and the solid precipitated was collected by filtration and dried under reduced pressure to obtain 2.23 g of N-(aminoiminomethyl)-3,4-dihydronaphthalene-2-carboxamide methanesulfonate.
Workup
- stirringThe resulting mixture was stirred at room temperature for 7 hours
- waitto stand overnight at room temperature
- extractionextracted twice with ethyl acetate
- washthe extract solution was washed twice with a 5% aqueous sodium chloride solution
- dry with materialdried over anhydrous magnesium sulfate
- distillationThe solvent was distilled off under reduced pressure
Sources & evidence
- ORD record
- ord-c8824d818ea445f485dd18bef5f1a17b
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06369110B1
Reaction notes
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