HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-(Morpholin-4-ylcarbonyl)-1-(propylsulfonyl)piperidine-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Propanesulfonyl chloride | HCID 66279 | — |
| Reactant | 4-(Morpholin-4-ylcarbonyl)piperidine-4-carbonitrile hydrochloride | HCID 68812963 | — |
| Solvent | diisopropylethylamine CH2Cl2 | HCID 21638731 | — |
| Product | 4-(Morpholin-4-ylcarbonyl)-1-(propylsulfonyl)piperidine-4-carbonitrile | HCID 57803089 | — |
Reaction Steps
To a solution of 4-(morpholin-4-ylcarbonyl)piperidine-4-carbonitrile hydrochloride (I-3) (10.40 g, 40 mmole) in DIEA-DCM (1:4, 200 mL) was added n-C3H7SO2Cl (6.28 g, 44 mmole) at 0° C. The resultant mixture was stirred for 1 h at 0° C. After this time, LCMS indicated that the reaction was complete. 2N NaOH (60 mL) was added to the reaction. The resultant reaction mixture was stirred for 1 h at rt. After this time, the DCM layer was separated. The aqueous solution was extracted with DCM (3×150 mL). The combined DCM solution was washed with brine, dried over MgSO4, filtered, and concentrated to afford the title compound (I-4) which was pure enough for next step reaction. Analytical LCMS: single peak (214 nm), 2.406 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576083B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-33398c38085549acb1b8bed782ebea1f |
| Source note | uspto-grants-2009_08 |