Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Glycolic Acid | HCID 757 | — |
| Reactant | HCID 22380577 | HCID 22380577 | — |
| Reactant | HCID 69719582 | HCID 69719582 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 22380566 | HCID 22380566 | 41% |
Reaction Steps
The 1-Ethoxycarbonyl-4-(1,3-dihydro-7-methyl-2H-benzimidazol-2-on-1-yl)piperidine (40 mg) obtained in Reference Example 11, (d) was dissolved in 5 N aqueous hydrochloric acid (0.8 ml), added with glycolic acid (16 mg) and stirred at 100° C. for 3 days. The reaction mixture was made alkaline by addition of aqueous ammonia and extracted twice with dichloromethane (2 ml). The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure to obtain 14.4 mg of the title compound. Yield: 41%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06916822B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-985121501c2649ddbede66f6323d8c3e |
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| Source note | uspto-grants-2005_07 |
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