HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → HCID 67052331, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | HCID 67052384 | HCID 67052384 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67052331 | HCID 67052331 | — |
Reaction Steps
Anhydrous hydrazine (0.160 mL, 5.22 mmol) was added to a suspension of N-[3-(4-amino-2-{[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]methyl}-1H-imidazo[4,5-c]-[1,5]naphthyridin-1-yl)propyl]-2-methylpropanamide (0.848 g, 1.74 mmol) in ethanol (10 mL). The mixture was allowed to stir at room temperature for 2.5 hours, then was concentrated under reduced pressure to yield crude N-(3-{4-amino-2-[(aminooxy)methyl]-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl}propyl)-2-methylpropanamide as a yellow solid, all of which was used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897767B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-6aec58cf05044638975a9fc43498a2a3 |
| Source note | uspto-grants-2011_03 |