Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(Dimethylamino)acetyl chloride hydrochloride | HCID 13994991 | — |
| Reactant | HCID 56591765 | HCID 56591765 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 56592556 | HCID 56592556 | — |
Reaction Steps
A suspension of 551 mg (1.5 mmol) 5-[2-(2-fluoro-phenyl)-[1,8]naphthyridin-4-yl]-[2,6]naphthyridin-1-ylamine in 10 ml DMF was treated with 108 mg (4.50 mmol) sodium hydride and stirred for 1 h at room temperature. Then 356 mg (2.25 mmol) dimethylaminoacetyl chloride hydrochloride were added and the reaction mixture was stirred for 18 h at room temperature. The reaction mixture was partitioned between water and dichloromethane. The organic phase was dried over sodium sulfate and evaporated. The residue was chromatographed on a silica gel column with ethyl acetate/methanol as eluent yielding 2-dimethylamino-N-{5-[2-(2-fluoro-phenyl)-[1,8]naphthyridin-4-yl]-[2,6]naphthyridin-1-yl}-acetamide as brown amorphous solid; HPLC/MS (B) 1.64 min, [M+H] 453.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08791113B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-de5505818f904f688f949726d5c8ddd8 |
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| Source note | uspto-grants-2014_07 |
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