HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850303Generated: October 30, 2026
Sodium Hydroxide → 2-Chloro-1,6-naphthyridine
https://huagongshe.com/reaction/1850303
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 1,6-Naphthyridin-2(1H)-One | HCID 589674 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Chloro-1,6-naphthyridine | HCID 13531967 | — |
Reaction Steps
A mixture of phosphoryl trichloride (5.17 ml, 56.5 mmol) and 1,6-naphthyridin-2(1H)-one (112) (1.65 g, 11.29 mmol, Alfa Aesar) was stirred at 70° C. for 16 h. The reaction mixture was cooled to RT and was poured onto 150 g of ice carefully. EtOAc (50 mL) was added and the mixture was treated carefully with about 30 mL of 5 M NaOH until the final pH is persistently >10. The mixture was vigorously mixed, then transferred into a separatory funnel. The EtOAc layer was then separated and dried and re-suspended in 30 mL of DCM, the insoluble solids were filtered off. The filtrate was loaded onto a silica gel pad and flushed with 30% EtOAc in hexanes to give a solid after drying. The solid was initially white but changed color to yellow after drying on the high vacuum line over night. Yield; 1.19 g, 64%. The material (113) was used directly in the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957073B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-7007f16cf82144508cde6d51a160adc0 |
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| Source note | uspto-grants-2015_02 |
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