Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2,4,6-Trimethyl-3-(pyrrolidin-1-yl)aniline | HCID 10798251 | — |
| Reactant | HCID 12547433 | HCID 12547433 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86596761 | HCID 86596761 | 35.6% |
Reaction Steps
To a solution of the 2,4,6-trimethyl-3-pyrrolidin-1-ylaniline (220 mg, 1.00 mmol) in of anhydrous dichloromethane (20 mL), were added pyridine (0.100 mL, 1.3 mmol) and 1-benzenesulfonyl-pyrrolidine-2-carbonyl chloride (0.297 g, 1.0 mmol). The reaction mixture was stirred overnight at room temperature. The solution was acidified with HCl (1N, 20 mL) and extracted with CH2Cl2 (2×20 mL). The combined organic layers were washed with a saturated aqueous solution of sodium bicarbonate (10 mL) and dried over magnesium sulfate (MgSO4). The organic layers were filtered and concentrated under reduced pressure to give a brown solid. The residue was further purified by flash chromatography (silica gel) using 95-5% hexane/ethyl acetate as the mobile phase (gradient) and semi-preparative HPLC to give ′1-(Phenylsulfonyl)-N-(2,4,6-trimethyl-3-pyrrolidin-1-ylphenyl)prolinamide (157 mg) as an off-white solid. MS m/z (M+H)+: calculated (m/z) 442.22, found (m/z) 442.25.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07579340B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-3e0e924396ea4019b2ccaf9ff0d90086 |
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| Source note | uspto-grants-2009_08 |
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