HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → N-(1-Adamantylmethyl)-5-chloro-2-(3-oxopropyl)isonicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(1-Adamantylmethyl)-5-chloro-2-(3-hydroxypropyl)isonicotinamide | HCID 21906688 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-(1-Adamantylmethyl)-5-chloro-2-(3-oxopropyl)isonicotinamide | HCID 21906722 | — |
Reaction Steps
To a stirred solution of N-(1-adamantylmethyl)-5-chloro-2-(3-hydroxypropyl)isonicotinamide (0.12 g, 0.33 mmol) (Example 14(ii)) in dry dichloromethane (10 mL) Dess-Martin periodinane (0.14 g, 0.33 mmol) was added. The resulting mixture was stirred at room temperature for 4 hours. The reaction was treated with diethyl ether (20 mL) and a saturated sodium bicarbonate solution containing sodium thiosulfate (0.37 g, in 4 mL). The mixture was stirred for 10 minutes and the organics separated; washed with brine (10 mL); dried over anhydrous magnesium sulfate; filtered; treated with acetic acid (0.30 mL) and concentrated. MS: APCI(+ve) 361, 363 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07129246B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-c8bba5c38fdd4e23a85948c3e6a25e68 |
| Source note | uspto-grants-2006_10 |