HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70798Generated: October 29, 2026
N-methyl-2-pyrrolidone → rel-11-[(3R,4S)-3-fluoro-4-(hydroxymethyl)-4-methoxypiperidin-1-yl]-2,2-dimethyl-2,3-dihydro-1H-cyclopenta[4,5]pyrido[1,2-a]benzimidazole-4-carboxamide
https://huagongshe.com/reaction/70798
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 11-chloro-2,2-dimethyl-2,3-dihydro-1H-cyclopenta[4,5]pyrido[1,2-a]benzimidazole-4-carboxamide | HCID 89413876 | — |
| Reactant | rel-[(3R,4S)-3-fluoro-4-methoxypiperidin-4-yl]methanol hydrochloride | HCID 89413909 | — |
| Solvent | Water | HCID 962 | — |
| Product | rel-11-[(3R,4S)-3-fluoro-4-(hydroxymethyl)-4-methoxypiperidin-1-yl]-2,2-dimethyl-2,3-dihydro-1H-cyclopenta[4,5]pyrido[1,2-a]benzimidazole-4-carboxamide | HCID 54588431 | 38.3% |
Reaction Steps
rel-[(3R,4S)-3-fluoro-4-methoxypiperidin-4-yl]methanol hydrochloride (399 mg) and DIPEA (523 μl) were added to an NMP (3 ml) solution of 11-chloro-2,2-dimethyl-2,3-dihydro-1H-cyclopenta[4,5]pyrido[1,2-a]benzimidazole-4-carboxamide (314 mg), and heating and stirring were performed at 200° C. for 60 minutes under microwave irradiation. After adding water to the reaction liquid, the resulting precipitate was collected by filtration and dried under reduced pressure. The resulting solid was purified by silica gel column chromatography (MeOH/chloroform). The resulting crude purified matter was washed with chloroform-EtOAc-hexane to obtain rel-11-[(3R,4S)-3-fluoro-4-(hydroxymethyl)-4-methoxypiperidin-1-yl]-2,2-dimethyl-2,3-dihydro-1H-cyclopenta[4,5]pyrido[1,2-a]benzimidazole-4-carboxamide (169 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822688B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-2e9ce635640d40b0acc324e8d119694a |
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| Source note | uspto-grants-2014_09 |
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