Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 178496783 | HCID 178496783 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178512478 | HCID 178512478 | 157.2% |
Reaction Steps
A solution of 2 g (0.0066 mole) of methyl 2-hydroxy-3-(1H-imidazol-4-ylmethyl)-benzenecarboximidate prepared in 6.a) above in 20 ml of methanol is added in one go to a solution of 1.52 ml (0.0033 mole) of hydrazine hydrate in 20 ml of methanol. The reaction is allowed to proceed for 15 minutes, then 40 ml of diethyl ether are added. The precipitate which has formed is filtered off and the filtrate is concentrated under reduced pressure. The evaporation residue is purified by preparative liquid chromatography (silica: 400 g; eluent: 89:10:1 (v/v/v) mixture of dichloromethane-methanol-ammonia). The pale yellow solid product obtained after evaporation of the solvents is recrystallized from methanol. 1.2 g of 2-hydroxy-3-(1H-imidazol-4-ylmethyl)-benzenecarboximidic acid hydrazide are obtained. Yield: 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05385927 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-79df7f302efd43168a8a02f34d25248d |
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| Source note | uspto-grants-1995_01 |
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