Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 18681145 | HCID 18681145 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18680815 | HCID 18680815 | 89.8% |
Reaction Steps
Four milliliters of acetic acid and 8 ml of ethanol were added to 0.434 g of N-(2-pyridylmethyl)-4-acetylamino-3-(4-benzyloxybenzylamino)benzamide, and the mixture was stirred at 90° C. for 7 hours. The reaction solution was concentrated under reduced pressure. Ethyl acetate and ether were added to the residue for crystallization. The crystals were separated through filtration, and were dried to give 0.375 g of 1-(4-benzyloxybenzyl)-2-methyl-6-[(2-pyridylmethyl)carbamoyl]benzimidazole (242).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06166219 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-ba719433a97941879cccb36193bb4e83 |
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| Source note | uspto-grants-2000_12 |
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