HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69057Generated: October 26, 2026
Sodium hydride → HCID 70656511, compound
https://huagongshe.com/reaction/69057
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Chloro-3-phenyl-1H-quinoline-2-one | HCID 2784810 | — |
| Reactant | 1-Ethyl-7-(3-iodopropoxy)-3,3,5-trimethyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione | HCID 68672792 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70656511 | HCID 70656511 | 42.8% |
Reaction Steps
4-Chloro-3-phenyl-1H-quinoline-2-one (0.3 g) was suspended in DMF (6 ml). Sodium hydride (60% in oil) (51 mg) was added, and the mixture was stirred for 15 minutes at room temperature. 1-Ethyl-7-(3-iodopropoxy)-3,3,5-trimethyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione (0.55 g) was added thereto and the mixture was stirred at room temperature for 7 days. The reaction mixture was poured to ice water (50 ml), and the generated insoluble matter was separated. The insoluble matter was dissolved in ethyl acetate. The liquid was dried over sodium sulfate and condensed under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1→1:3). The purified product was condensed under reduced pressure, and the residue was recrystallized from ether, thereby obtaining the title compound (0.28 g) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08822453B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-eddda42932b94501a13323774f1500a5 |
|---|
| Source note | uspto-grants-2014_09 |
|---|