HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Ethylamino)ethanol → 2-[{2-[6-amino-5-(methyloxy)-2,3-dihydro-1H-indol-1-yl]-2-oxoethyl}(ethyl)amino]ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Ethylamino)ethanol | HCID 8072 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(bromoacetyl)-5-(methyloxy)-6-nitro-2,3-dihydro-1H-indole | HCID 59441834 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[{2-[6-amino-5-(methyloxy)-2,3-dihydro-1H-indol-1-yl]-2-oxoethyl}(ethyl)amino]ethanol | HCID 59441958 | 101.2% |
Reaction Steps
The 1-(bromoacetyl)-5-(methyloxy)-6-nitro-2,3-dihydro-1H-indole (4.0 g, 12.7 mmol) was dissolved in 50 mL of dicholomethane, then K2CO3 (4.4 g, 31.7 mmol) and 2-(ethylamino)ethanol (2.3 g, 25.4 mmol) in 10 mL dichloromethane were added, the reaction was stirred at RT for 3 hours. After filtration, the organic layers were washed with water (2×100 mL)and dried over Na2SO4. The solvent was removed to yield the 2-[{2-[6-amino-5-(methyloxy)-2,3-dihydro-1H-indol-1-yl]-2-oxoethyl}(ethyl)amino]ethanol as a yellow solid (3.77 g, 92%).1HNMR (400 MHz, DMSO-d6) δ ppm: 0.94 (t, J=7.14 Hz,3 H), 2.45 (s, 2 H), 2.60 (m, 4 H), 3.18 (t, J=8.42 Hz, 2 H), 3.40 (t, J=6.13 Hz,2H), 3.84 (s, 3 H), 4.19 (t, J=8.51 Hz, 2 H), 7.29 (s, 1 H), 8.43 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07981903B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-fecab98984bb444c944e18c3d09c71f3 |
| Source note | uspto-grants-2011_07 |