HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(2-Bromoethoxy)salicylamide → Cgp-20712
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(2-Bromoethoxy)salicylamide | HCID 13754420 | — |
| Reactant | 1-amino-3-[4-(1-methyl-4-(trifluoromethyl)-1H-imidazol-2-yl)-phenoxy]-2-propanol | HCID 20255196 | — |
| Product | Cgp-20712 | HCID 2685 | — |
Reaction Steps
A mixture of 1.5 g of 1-amino-3-[4-(1-methyl-4-(trifluoromethyl)-1H-imidazol-2-yl)-phenoxy]-2-propanol and 0.82 g of 5-(2-bromoethoxy)-salicylamide is stirred for 1 hour in an oil bath at a temperature of 100°. The melt is then extracted by boiling with 30 ml of isopropanol. The filtered solution is concentrated to 15 ml, cooled and the crystals that are precipitated are filtered off. Recrystallisation from methanol yields 1-[2-(3-carbamoyl-4-hydroxyphenoxy)-ethylamino]-3-[4-(1-methyl-4-(trifluoromethyl)-1H-imidazol-2-yl)-phenoxy]-2-propanol having a melting point of 195°-197°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04559354 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-6b30949cae6f45b78386ba4048b8c0ef |
| Source note | uspto-grants-1985_12 |