HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → HCID 68539374, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | HCID 68539763 | HCID 68539763 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68539374 | HCID 68539374 | 135% |
Reaction Steps
Anhydrous hydrazine (94 mg, 2.96 mmol) was added to 2-[4-(4-amino-6,7,8,9-tetrahydro-1H-imidazo[4,5-c]quinolin-1-yl)butoxy]-1H-isoindole-1,3(2H)-dione (600 mg, 1.48 mmol) in ethanol (25 mL) at ambient temperature. The reaction was stirred overnight, and additional hydrazine (2 equivalents) was added. After stirring for 2 hours at ambient temperature, the reaction was concentrated under reduced pressure. The residue was diluted with dichloromethane and concentrated under reduced pressure three times to remove the hydrazine and then dried under vacuum to provide 550 mg of impure 1-[4-(aminooxy)butyl]-6,7,8,9-tetrahydro-1H-imidazo[4,5-c]quinolin-4-amine as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07648997B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-6089199b34b24d29a8c553382a019f96 |
| Source note | uspto-grants-2010_01 |