HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-[(1-methylpyrrolidin-3-yloxy)phenyl-methyl]-1H-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-(alpha-Hydroxybenzyl)benzimidazole | HCID 5792 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Methyl-3-pyrrolidinol | HCID 93074 | — |
| Solvent | Methanesulfonic Acid | HCID 6395 | — |
| Product | 2-[(1-methylpyrrolidin-3-yloxy)phenyl-methyl]-1H-benzimidazole | HCID 66835867 | — |
Reaction Steps
A mixture of (1H-benzimidazol-2-yl)phenylmethanol (611 mg) and 1-methyl-3-pyrrolidinol (263 mg) in methanesulfonic acid (1.3 mL) is heated for 4 hours in a sealed tube at a temperature close to 140° C. The mixture is cooled back to room temperature, poured into water which is then made alkaline with concentrated sodium hydroxide solution. The aqueous phase is extracted with ethyl acetate. Pooled extracts are dried over magnesium sulfate, concentrated under reduced pressure. The residue is purified by column chromatography over silica gel (gradient dichloromethane/methanol from 100/0 to 90/10) to give 2-[(1-methylpyrrolidin-3-yloxy)phenyl-methyl]-1H-benzimidazole melting at 53° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029357B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-dc692da432f04e48b33a298f6f060cd7 |
| Source note | uspto-grants-2015_05 |