HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382363Generated: October 25, 2026
Sodium Hydroxide → 1-benzyl-4-amino-1H-imidazole-5-carboxamide
https://huagongshe.com/reaction/382363
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Amino-1-benzyl-5-imidazole carboxamide hydrochloride | HCID 18360336 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-benzyl-4-amino-1H-imidazole-5-carboxamide | HCID 14000620 | 94.2% |
Reaction Steps
9.12 g (30 mol) of 4-benzylideneamino-1-benzyl-5-imidazolecarboxamide obtained was dissolved in 135 ml of tetrahydrofuran. After the addition of 15 ml of concentrated hydrochloric acid, the mixture was stirred at room temperature for two hours. The precipitate obtained was separated by filtration and washed with tetrahydrofuran to obtain 7.26 g of 4-amino-1-benzyl-5-imidazolecarboxamide hydrochloride. 7.26 g of the 4-amino-1-benzyl-5-imidazole carboxamide hydrochloride obtained was dissolved in a mixed solvent of 100 ml of methyl alcohol and 80 ml of distilled water. After the addition of 7.5 ml of 4 N aqueous solution of sodium hydroxide, the mixture was stirred at room temperature for one hour. Methanol was evaporated and the resulting precipitate separated by filtration was washed with distilled water and ethanol to obtain 5.85 g of the title compound (yield 90%) (2 steps).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310070B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-83f0dc67c0154cc49a566396b89ae717 |
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| Source note | uspto-grants-2001_10 |
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