HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(6-chloroimidazo[1,2-b]pyridazin-2-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-6-chloroimidazo[1,2-b]pyridazine | HCID 49758021 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(6-chloroimidazo[1,2-b]pyridazin-2-yl)acetamide | HCID 59519510 | 66.9% |
Reaction Steps
To a solution of 6-chloroimidazo[1,2-b]pyridazin-2-amine (18 g, 106.5 mmol) in DCM (180 mL) was added triethylamine (10.8 g, 106.5 mmol), DMAP (1.32 g, 1.06 mmol), and acetic anhydride (6 g, 106.5 mmol) sequentially at rt. The reaction mixture was stirred for 5 h at rt and the precipitate was filtered and washed with 50 mL of methanol to afford the title compound (15 g, 66%). 1H NMR (DMSO-d6, 300 MHz): δ 7.3 (d, 1H), 8.02 (d, 1H), 8.25 (s, 1H). LCMS (M+1) 211 (99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820665B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-174b31240f82450282c5297214fcc8c1 |
| Source note | uspto-grants-2010_10 |