Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | dimethoxytetrahydrofurane | HCID 11788317 | — |
| Reactant | HCID 22386994 | HCID 22386994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 66725717 | HCID 66725717 | 39.4% |
Reaction Steps
In a three necked flask, under argon, a suspension of 2-[4-amino-2-oxo-1-pyrrolidinyl]butanamide 393 (6.99 g, 0.037 mol.), dimethoxytetrahydrofurane (5.53 g, 0.041 mol.), pyridine (50.6 ml) and AcOH (36 ml) is warmed to 70° C. and dissolution occurs. After 2 h at this temperature, the reaction is cooled down to room temperature, concentrated in vacuo and the crude product is purified by chromatography on silicagel (CH2Cl2/MeOH: 95/05 (v/v)) to afford 223 as an oil (2.67 g, 30.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06806287B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-6115764402b54b248225ad88916620f3 |
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| Source note | uspto-grants-2004_10 |
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