HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triacetoxyperiodinane → 1-(1-(5-(2-Fluorophenyl)pyrimidin-2-yl)-6-(morpholine-4-carbonyl)-1H-indol-3-yl) ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | (1-(5-(2-Fluorophenyl)pyrimidin-2-yl)-3-(1-hydroxyethyl)-1H-indol-6-yl)(morpholino)-methanone | HCID 118666316 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(1-(5-(2-Fluorophenyl)pyrimidin-2-yl)-6-(morpholine-4-carbonyl)-1H-indol-3-yl) ethanone | HCID 131735395 | — |
Reaction Steps
Dess-Martin periodinane reagent (437 mg, 1.008 mmol, 1.5 eq) was added at 0° C. to a stirred solution of (1-(5-(2-fluorophenyl)pyrimidin-2-yl)-3-(1-hydroxyethyl)-1H-indol-6-yl)(morpholino)methanone (synthesis example 28, 300 mg, 0.672 mmol, 1.0 eq) in dichloromethane (10 mL). Stirring was continued for 2 h at room temperature and the reaction mixture was then filtered through a bed of celite. The celite was washed with dichloromethane (10 mL) and the filtrate was dried over anhydrous sodium sulfate and evaporated in vacuo. White solid. Yield: 250 mg (72% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09315490B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-ad465f978c3841f0a5c332051036fd71 |
| Source note | uspto-grants-2016_04 |