HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 23557335, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 2-bromohexanoate | HCID 79072 | — |
| Reactant | HCID 12107974 | HCID 12107974 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23557335 | HCID 23557335 | 69.6% |
Reaction Steps
To a solution of N,N′-di-quinolin-8-yl-malonamide (10.3 g, 28.8 mmol) in dry DMF (200 mL) and dry THF (85 mL) at 0° C. was added NaH (60% disp./1.27 g, 31.7 mmol) portion-wise. The resultant solution was allowed to warm to RT for 10 min. The solution was cooled to 0° C. and ethyl bromohexanoate (5.6 mL, 31.7 mmol) was added dropwise. The mixture was stirred overnight. The solvent was removed, and the residue was diluted with EtOAc (250 mL), and washed with H2O (100 mL). The organic fraction was dried, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography to yield the desired material (10 g, 69.6%). ESIMS calcd 499 (M++H), found 499 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08158825B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-106981c0e3bd46e197babcd59da7b39f |
| Source note | uspto-grants-2012_04 |