HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914821Generated: October 31, 2026
Potassium Carbonate → HCID 58034515, compound
https://huagongshe.com/reaction/1914821
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl {1-[4-(phenylacetyl)phenyl]cyclobutyl}carbamate | HCID 57805516 | — |
| Reactant | tert-Butyl (2-chloro-4-formylpyridin-3-yl)carbamate | HCID 58034339 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58034515 | HCID 58034515 | — |
Reaction Steps
A mixture of tert-butyl (2-chloro-4-formylpyridin-3-yl)carbamate (7-3) (300 mg, 1.17 mmol), tert-butyl {1-[4-(phenylacetyl)phenyl]cyclobutyl}carbamate (4-1) (427 mg, 1.17 mmol) and potassium carbonate (485 mg, 3.51 mmol) in DMF (10 mL) was stirred at 120° C. for 15 hours. The reaction mixture was cooled to room temperature, diluted with ethyl acetate, washed with water, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (hexane-EtOAc) to give tert-butyl {1-[4-(8-chloro-3-phenyl-1,7-naphthyridin-2-yl)phenyl]cyclobutyl}carbamate (7-4) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614221B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-66d1d7325bce42c9a4f85efebaa68ca5 |
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| Source note | uspto-grants-2013_12 |
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