HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 59145191, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 2-((1,1-Dimethylethyl)imino)-N,N-diethylhexahydro-1,3-dimethyl-2lambda5-1,3,2-diazaphosphorin-2-amine | HCID 3513851 | — |
| Reactant | HCID 68536565 | HCID 68536565 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59145191 | HCID 59145191 | — |
Reaction Steps
To a solution of N-{2-[benzoyl(3,3-diphenylpropyl)amino]ethyl}-4-indolinecarboxamide (77.0 mg) and 2-(tert-butylimino)-2-diethylamino-1,3-dimethylperhydro-1,3,2-diazaphosphorine (106 μL) in DMF (2.3 mL) was added ethyl bromoacetate (39 μL) and the mixture was stirred at ambient temperature for 40 hours. The resulting mixture was diluted with EtOAc (20 mL), washed successively with 1M HCl aqueous solution, saturated NaHCO3 aqueous solution and brine, dried over anhydrous MgSO4, filtered and evaporated in vacuo. The residue was purified by silica gel column chromatography (chloroform: MeOH=99:1) to afford ethyl {4-[({2-[benzoyl(3,3-diphenylpropyl)amino]ethyl}amino)-carbonyl]-2,3-dihydro-1H-indol-1-yl}acetate (87 mg) as an yellow syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273745B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-06364e57b4fd40cabf427eb6e7208ba3 |
| Source note | uspto-grants-2012_09 |