HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-((4-(2-(Cyclopropylmethoxy)ethyl)phenoxy)methyl)oxirane → 1-[N-[2-(3-carbamoyl-4-hydroxy-phenoxy)-ethyl]-benzylamino]-3-[4-[2-(cyclopropylmethoxy)ethyl]-phenoxy]-2-propanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-((4-(2-(Cyclopropylmethoxy)ethyl)phenoxy)methyl)oxirane | HCID 11791542 | — |
| Reactant | 5-(2-Benzylaminopropoxy)salicylamide | HCID 13754334 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-[N-[2-(3-carbamoyl-4-hydroxy-phenoxy)-ethyl]-benzylamino]-3-[4-[2-(cyclopropylmethoxy)ethyl]-phenoxy]-2-propanol | HCID 20151321 | — |
Reaction Steps
A solution of 14.3 g of 1-[2-(cyclopropyl-methoxy)-ethyl]-4-(2,3-epoxypropoxy)-benzene (German Offenlegungsschrift No. 2,649,605) and 16.3 g of 5-[2-(benzylamino)-propoxy]-salicylamide in 200 ml of isopropanol is refluxed for 18 hours. The reaction mixture is concentrated by evaporation to leave crude 1-[N-[2-(3-carbamoyl-4-hydroxyphenoxy)-ethyl]-benzylamino]-3-[4-[2-(cyclopropylmethoxy)-ethyl]-phenoxy]-2-propanol in the form of brown oil, which can be further processed without additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04497813 |
| Source dataset | uspto-grants-1985_02 |
| ORD ID | ord-c7e4511312f344bdb523e33a6262229f |
| Source note | uspto-grants-1985_02 |