HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 4-Benzyloxy-1-cyclopropylmethyl-3-iodo-1H-pyridin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 4-(Benzyloxy)-1-(cyclopropylmethyl)pyridin-2(1H)-one | HCID 59497099 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Benzyloxy-1-cyclopropylmethyl-3-iodo-1H-pyridin-2-one | HCID 59497102 | 92.1% |
Reaction Steps
N-Iodosuccinimide (2.64 g, 11.74 mmol) was added to a solution of intermediate D1 (3.0 g, 11.74 mmol) in acetic acid (40 ml). The reaction mixture was stirred at room temperature for 1 hour, after which it was concentrated in vacuo. The residue was purified by column chromatography (silica gel; DCM as eluent) and finally recrystallized from diethyl ether to yield intermediate D6 (4.12 g, 92%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08748621B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-a81ac2ea9b8741c5813366efb56c05ac |
| Source note | uspto-grants-2014_06 |