HuagongsheHuagongshe Chemistry Print Report · For research reference only
Guanidine → HCID 178464068, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Guanidine | HCID 3520 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 15388932 | HCID 15388932 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178464068 | HCID 178464068 | — |
Reaction Steps
1.5 g of CDI are added to a suspension of 2.0 g of 6-(2-diethylaminoethoxy)-1-naphthoic acid in 50 ml of THF, and the reaction mixture is stirred at RT overnight. It is then treated with 2.0 g of guanidine, again stirred overnight and concentrated, and the residue is stirred with 100 ml of water. The precipitate formed is filtered off with suction and purified by FC using methylene chloride/methanol 1:1.0.66 g of 6-(2-diethylaminoethoxy)-1-naphthoylguanidine is obtained; m.p.: 168-169° C. 1H-NMR (DMSO-d6): δ [ppm]=1.0 (6H), 2.6 (4H), 2.85 (2H), 4.15 (2H), 7.15 (1H), 7.3 (1H), 7.4 (1H), 7.75 (2H), 8.7 (1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06600072B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-afe7abf3d44b4bfe9fe7c63c02f3f4e6 |
| Source note | uspto-grants-2003_07 |