| Identification | Back Directory | [Name]
(5-AMINO-1H-1,2,4-TRIAZOL-3-YL)METHANOL | [CAS]
63870-39-3 | [Synonyms]
NSC513582 ZERO/004602 ZINC02415220 ASINEX-REAG BAS 03825303 (3-Amino-1H-1,2,4-triazol-5-yl) (5-AMINO-1H-1,2,4-TRIAZOL-3-YL)METHANOL (5-amino-2H-1,2,4-triazol-3-yl)methanol methanol compound with 2-hydroxyacetic acid (3-AMINO-1H-1,2,4-TRIAZOL-5-YL)METHANOL 2-HYDROXYACETIC ACID (3-AMino-1H-1,2,4-triazol-5-yl)Methanol coMpound with 2-hydroxyacetic acid Acetic acid, hydroxy-, compd. with 5-amino-1H-1,2,4-triazole-3-methanol (1:1) | [Molecular Formula]
C3H6N4O | [MDL Number]
MFCD02933180 | [MOL File]
63870-39-3.mol | [Molecular Weight]
114.11 |
| Hazard Information | Back Directory | [Synthesis]
Aminoguanidine bicarbonate (23.5 g, 172 mmol) was added in batches to a mixture of ethanoic acid (26.2 g, 345 mmol) and water (10 mL) over a period of 0.1 hours. During the addition, the reaction mixture was gently heated to maintain the internal temperature at 25 °C. Subsequently, concentrated nitric acid (1.0 mL) was added slowly and dropwise to the reaction system, and then the reaction mixture was heated to an internal temperature of 104-108 °C over 22 hours. Upon completion of the reaction, the heating was stopped and the solution was allowed to cool naturally with stirring. The slurry cooled to 10 °C was continued to be stirred for 2 h. Subsequently, it was filtered and the filter cake was washed with ethanol (EtOH). The resulting solid was dried overnight under vacuum to afford the target product (5-amino-1H-1,2,4-triazol-3-yl) methanol ethanolate (Product 88a, 29.5 g, 85% yield). Mass spectrometry analysis: calculated value (M + H)+ = 115, measured value (M + H)+ = 115. | [References]
[1] Patent: WO2012/83105, 2012, A1. Location in patent: Page/Page column 101 [2] Patent: WO2007/23381, 2007, A1. Location in patent: Page/Page column 54-55 [3] Patent: WO2004/74270, 2004, A2. Location in patent: Page 300 [4] Patent: US2005/176701, 2005, A1. Location in patent: Page/Page column 144 |
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