HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isatoic Anhydride → HCID 178507502, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isatoic Anhydride | HCID 8359 | — |
| Reactant | HCID 178419017 | HCID 178419017 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178507502 | HCID 178507502 | 14.3% |
Reaction Steps
The subtitled compound was prepared substantially in accordance with the method detailed in Example 6A using 5.55 g (0.05 mol) of 4-(2-aminoethyl)imidazole in 40 ml ethanol and 8.31 g (0.05 mol) of isatoic anhydride with the exception that after removing ethanol from the reaction solution the product was purified using column chromatography (500 ml dichloromethane; 2000 ml 9% methanol in dichloromethane, isocratic eluent). The fractions containing the desired product were combined and reduced to dryness under reduced pressure to provide a solid. This solid was recrystallized from diethyl ether to provide 1.65 g of the desired subtitled compound (m.p. 85°-87° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05397798 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-dcd1f6ec798e41efaf398ec653ce43ce |
| Source note | uspto-grants-1995_03 |