HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → 7-(Pyridin-2-yl-quinolin-2-yl-amino)-heptanoic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 7-bromoheptanoate | HCID 122490 | — |
| Reactant | 2-Pyridyl-2-quinolylamine | HCID 5340112 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-(Pyridin-2-yl-quinolin-2-yl-amino)-heptanoic acid ethyl ester | HCID 58545023 | 55% |
Reaction Steps
NaH (35 mg, 0.91 mmol) was added to II (344 mg, 0.91 mmol) in DMF (5 mL) at rt. After 10 min, KI (227 mg, 1.37 mmol) and ethyl 7-bromoheptanoate (0.267 mL, 1.37 mmol) were added. The reaction mixture was stirred at 90° C. for 19 h after which 0.1 M Na2S2O3 (50 mL) and EtOAc (50 mL) were added; the phases were then separated and the aqueous phase extracted with EtOAc (2×25 mL). The organic phases were combined then dried over MgSO4, filtered, and subsequently evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography, eluting with hexane/EtOAc (90:10 to 85:15), to furnish III as a colourless oil (189 mg, 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09340503B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-c24b48f5ff2f439ba98f8b2199042960 |
| Source note | uspto-grants-2016_05 |