HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline → HCID 18790420, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline | HCID 27833 | — |
| Reactant | 1,4,7,10,13,16-Hexaazacyclooctadecane | HCID 41779 | — |
| Reactant | N-Benzyloxycarbonyl-beta-alanine | HCID 75313 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18790420 | HCID 18790420 | — |
Reaction Steps
516 mg (2 mmol) of 1,4,7,10,13,16-hexaazacyclooctadecane (hexacyclene; Fluka) is azeotropically dehydrated with toluene. A solution of 3.35 g (15 mmol) of benzyloxycarbonyl-β-alanine (Sigma) in tetrahydrofuran (THF) as well as 3.71 g (15 mmol) of 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline (EEDQ; Fluka) are added to the cooled solution of hexacyclene in toluene at room temperature and stirred overnight. After the reaction is completed, the product is precipitated by adding hexane, and the precipitate is chromatographed on silica gel with dichloromethane/hexane/isopropanol (20:10:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06057419 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-4071472a056e4f2693dc43a5ae81ec8e |
| Source note | uspto-grants-2000_05 |