HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42369Generated: October 29, 2026
Dimethylformamide → HCID 58216598, compound
https://huagongshe.com/reaction/42369
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl {1-[4-(phenylacetyl)phenyl]cyclobutyl}carbamate | HCID 57805516 | — |
| Reactant | tert-Butyl (6-chloro-2-formylpyridin-3-yl)carbamate | HCID 58216578 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58216598 | HCID 58216598 | — |
Reaction Steps
To a round bottom flask was added tert-butyl {1-[4-(phenylacetyl)phenyl]cyclobutyl}carbamate (1-3) (2.7 g, 6.1 mmol), tert-butyl (6-chloro-2-formylpyridin-3-yl)carbamate (1-4) (1.6 g, 6.1 mmol), potassium carbonate (5.0 g, 6.0 mmol), and DMF (20 mL). The reaction mixture was heated to 80° C. while stirring in a hot oil bath under an atmosphere of nitrogen for 15 hours. Then the reaction mixture was warmed to 120° C. for 1 hour. The reaction mixture was permitted to cool to room temperature, added water, suspended in ethyl acetate, washed with a saturated solution of sodium bicarbonate, followed by water, brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The resulting residue was purified by silica gel chromatography (5-50% EtOAc/5% DCM/Hexane) to give tert-butyl {1-[4-(6-chloro-3-phenyl-1,5-naphthyridin-2-yl)phenyl]cyclobutyl}carbamate (1-5) as an off-white solid. HRMS (M+H)+: observed=486.1954, calculated=486.1943.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536193B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-cb2a375574994237b62a87a93fcd5f83 |
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| Source note | uspto-grants-2013_09 |
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