HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 1-(3-((4-nitro-1H-indazol-1-yl)methyl)piperidin-1-yl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-nitro-1-(piperidin-3-ylmethyl)-1H-indazole | HCID 67976102 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(3-((4-nitro-1H-indazol-1-yl)methyl)piperidin-1-yl)ethanone | HCID 67974591 | 52.4% |
Reaction Steps
A solution of 4-nitro-1-(piperidin-3-ylmethyl)-1H-indazole (0.050 g, 0.139 mmol), triethylamine (0.097 mL, 0.699 mmol) in DCM (1 mL) was treated with acetic anhydride (0.0158 mL, 0.168 mmol) at ambient temperature and stirring continued for 1 hour. The mixture was quenched with saturated aqueous sodium bicarbonate, extracted with DCM, dried (phase separator silicone treated filter paper) and concentrated to provide 1-(3-((4-nitro-1H-indazol-1-yl)methyl)piperidin-1-yl)ethanone (0.022 g, 52% yield) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09174981B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-4401c4df7ecc4bcdb731aef308c135d0 |
| Source note | uspto-grants-2015_11 |