HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408005Generated: October 30, 2026
Diisopropylethylamine → HCID 67469768, compound
https://huagongshe.com/reaction/408005
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Chloro-2,3-difluoropyridine | HCID 2783248 | — |
| Reactant | (S)-methyl 3-fluoro-4-(2-oxo-1-(piperidin-4-yl)pyrrolidin-3-yloxy)benzoate hydrochloride | HCID 67469793 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67469768 | HCID 67469768 | 54.6% |
Reaction Steps
To a solution of (S)-methyl 3-fluoro-4-(2-oxo-1-(piperidin-4-yl)pyrrolidin-3-yloxy)benzoate hydrochloride (Example 151, Step B; 2.0 g, 5.9 mmol) in DMF (3 mL) was added N-ethyl-N-isopropylpropan-2-amine (3.8 g, 30 mmol) and 5-chloro-2,3-difluoropyridine (2.7 g, 18 mmol) and the reaction was heated to 60° C. overnight. The reaction was next diluted with EtOAc (30 mL) and washed with water (30 mL), and brine (30 mL), and the combined organic phases were dried over MgSO4, filtered and concentrated under vacuum. The crude material was purified on silica using a gradient of DCM to 1:19 EtOAc:DCM as eluent to yield (S)-methyl 4-(1-(1-(5-chloro-3-fluoropyridin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-yloxy)-3-fluorobenzoate (1.5 g, 54%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754226B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-afc7fc35376a40339af74e232a43d22f |
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| Source note | uspto-grants-2014_06 |
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