HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → HCID 86622763, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 58055059 | HCID 58055059 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86622763 | HCID 86622763 | — |
Reaction Steps
1-(3,4-dichlorobenzyl)-3-(4-(iodomethyl)thiazol-2-yl)urea (Intermediate XXII) was taken up in THF and an excess of the 2-Amino-ethanol (20 equiv.) was added. The reaction was allowed to stir overnight at room temperature. Reaction poured into water and extracted with ethyl acetate, partitioned with brine, dried over NaSO4, filtered, and volatiles were removed in vacuo. The resulting solid was triturated with ethyl acetate, followed by diethyl ether to give the title compound. 1H NMR (400 MHz, CD3OD): 7.50-7.45 (m, 2H), 7.26 (dd, 1H), 6.78 (s, 1H), 4.41 (s, 2H), 3.73 (s, 2H), 3.65 (t, 2H), 2.71 (t, 2H). MS (ES+): M/Z 375 and 377 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08716320B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-0bcf118631424f68ac5b317637b6f4e4 |
| Source note | uspto-grants-2014_05 |