HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium diisopropylamide → 7-bromo-3-chloro-1-fluoro-5H-chromeno[2,3-c]pyridin-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Tetrahydrofuran heptane ethylbenzol | HCID 22742125 | — |
| Reactant | HCID 86640732 | HCID 86640732 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-bromo-3-chloro-1-fluoro-5H-chromeno[2,3-c]pyridin-5-one | HCID 57475642 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To a solution of 5-bromo-2-(6-chloro-2-fluoropyridin-3-yloxy)-N,N-diethylbenzamide (120 mg, 0.299 mmol) in 5 mL of dry THF at −78° C. was added dropwise lithium diisopropylamide, 2.0M heptane/THF/ethylbenzene (158 μL, 1.195 mmol) (0.6 mL of 2M solution) and the reaction was stirred at −78° C. for 3 h. The reaction was quenched at −78° C. with sat. NH4Cl and was allowed to warm up to RT. The reaction was extracted with ETOAc, dried over Na2SO4, filtered and evaporated to dryness. The crude was purified by column chromatography (1:1 hexane/DCM to 100% DCM) to give the titled compound, 7-bromo-3-chloro-1-fluoro-5H-chromeno[2,3-c]pyridin-5-one, as an offwhite solid. MS (M+1): 328.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08962859B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-292ef61033a547029fd7f788d58d8c3a |
| Source note | uspto-grants-2015_02 |