Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-(1,3-Dioxolan-2-yl)-6-fluoropyridine | HCID 10559050 | — |
| Product | HCID 19361727 | HCID 19361727 | — |
Reaction Steps
0.60 g of 2-[1,3]dioxolan-2-yl-6-fluoropyridine (3.55 mmol) and 2.50 ml of dimethylamine at 33% in ethanol (17.7 mmol) are mixed and then the mixture is heated at the temperature of 100° C. for 12 hours. After evaporation under vacuum, the residue is taken up in chloroform, the mixture is washed with water, dried over magnesium sulfate, filtered and the chloroform is evaporated under vacuum. The title product is obtained in the form of a yellow oil which is used in the next stage without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06020345 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-ee1a931f0a58437eb81d608819e5a7f8 |
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| Source note | uspto-grants-2000_02 |
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