Methanol → 5-(4-methoxybenzyl)-1H-1,2,4-triazol-3-amine
Reaction equation
[N+]([O-])(O)=O.[NH2:5][NH:6][C:7]([NH2:9])=[NH:8].CO.C[O-].[Na+].[CH3:15][O:16][C:17]1[CH:22]=[CH:21][C:20]([CH2:23][C:24](OC)=O)=[CH:19][CH:18]=1>O>[CH3:15][O:16][C:17]1[CH:22]=[CH:21][C:20]([CH2:23][C:24]2[NH:5][N:6]=[C:7]([NH2:9])[N:8]=2)=[CH:19][CH:18]=1Participants
Conditions
- Temperature
- 0 °C
Procedure
To a stirred mixture of N-aminoguanidine nitrate (5.50 g, 40 mmol) and anhydrous methanol (50 mL) cooled to 0 C was added sodium methoxide solution (25% in methanol, 9.2 mL, 40 mmol) dropwise. The resulting mixture was stirred at 0° C. for 10 min before methyl 2-(4-methoxyphenyl)acetate (1.6 mL, 10 mmol) was added. The mixture was then stirred at 0° C. for 10 min, RT for 10 min, and 75° C. for 27 hr. The reaction mixture was cooled and diluted with 20 mL of water. Methanol was removed under vacuum and the aqueous solution was acidified to pH=3-4 with 3 N aqueous HCl solution. The solid obtained was filtered, washed with water, and recrystalized in ethanol-water to give 1.65 g (81% yield) of 5-(4-methoxybenzyl)-1H-1,2,4-triazol-3-amine as a white solid. (M+H)+=205.22
Workup
- temperaturecooled to 0 C
- additionwas added
- wait75° C. for 27 hr
- temperatureThe reaction mixture was cooled
- customMethanol was removed under vacuum
- customThe solid obtained
- filtrationwas filtered
- washwashed with water
- customrecrystalized in ethanol-water
Sources & evidence
- ORD record
- ord-6aacd4c287364ded95923b186c7146ef
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07361654B2
Reaction notes
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