Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorine monoxide | HCID 24646 | — |
| Reactant | Sodium potassium tartrate tetrahydrate | HCID 2724148 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 1-benzyl-1H-[1,2,4]triazole-3-carboxylic acid cyclohexylamide | HCID 67023585 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | (1-benzyl-1H-[1,2,4]triazol-3-ylmethyl)-cyclohexyl-amine | HCID 67023661 | — |
Reaction Steps
A solution of 1-benzyl-1H-[1,2,4]triazole-3-carboxylic acid cyclohexylamide (3.63 g, 12.8 mmol) in phosphosphorus oxychloride (10 mL) was heated at 70° C. for 4 hours. The solution was then concentrated. Toluene was added and then evaporated. The residue was dissolved in THF (100 mL). The solution was cooled to 0° C., and LiAlH4 (1.0 M in THF, 25.6 mL, 25.6 mmol) was added slowly into the solution. The solution was allowed to return to room temperature and then stirred for 1 hour. Potassium sodium tartrate tetrahydrate (5 g) was added. Water was added slowly to terminate the reaction. The solution was filtered and ethyl acetate was used to wash the filter cake. The filtrate was concentrated. HCl (1.0 M) in diethyl ether was added. The resulting precipitate was collected and recrystallized from acetone/methanol to yield (1-benzyl-1H-[1,2,4]triazol-3-ylmethyl)-cyclohexyl-amine as its corresponding hydrochloric acid salt, as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531545B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-420fc4034f9d46789a6038938521cdef |
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| Source note | uspto-grants-2009_05 |
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