HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712652Generated: October 28, 2026
Ethyl Acetate → 6-(5-Dimethylcarbamoylmethyl-pyridin-3-yl)-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid amide
https://huagongshe.com/reaction/712652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-(5-bromopyridin-3-yl)-N,N-dimethylacetamide | HCID 53785079 | — |
| Reactant | 6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid amide 1,4-dioxane | HCID 131733988 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-(5-Dimethylcarbamoylmethyl-pyridin-3-yl)-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid amide | HCID 117666991 | 7.9% |
Reaction Steps
2-(5-Bromo-pyridin-3-yl)-N,N-dimethyl-acetamide (73 mg, 0.30 mmol) and 2.0 M Na2CO3 aqueous solution (0.30 mL, 0.60 mmol) are added into the crude 6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid amide 1,4-dioxane solution (3.0 mL, 0.36 mmol) which is synthesized according to the procedure for Step 3 of Example 16. The Argon gas is bubbled through the solution for 5 min. Then PdCl2dppf (11 mg, 0.015 mmol) is added. The mixture is heated at 100° C. for 3.5 hrs before EtOAc (15 mL) and water (15 mL) are added. The aqueous layer is separated and extracted with EtOAc (2×10 mL). The organic layers are combined and concentrated to give the crude product. Purification by flash column chromatography affords 8.0 mg of the titled product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09181272B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-ec619efa9afa458ebc4b8e7e44bc6e5f |
|---|
| Source note | uspto-grants-2015_11 |
|---|