Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Ethyl 6-chloronicotinate | HCID 2799611 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 6-morpholinonicotinate | HCID 14297054 | — |
Reaction Steps
Ethyl 6-chloronicotinate (5.0 g) and morpholine (10 ml) were mixed and then heated to 100° C. In less than 5 minutes at this temperature, a thick paste formed. Acetonitrile (15 ml) was added and heating was continued overnight at 90° C. The mixture was cooled, diluted with water and extracted with ethyl acetate. The organic layer was dried and concentrated in vacuo to give ethyl 6-morpholin-4-ylpyridine-3-carboxylate as a white solid. NMR (300 MHz, CDCl3: 8.80 (s, 1H), 8.05 (d, 1H), 6.60 (d, 1H), 4.35 (q, 2H), 3.80 (m, 4H), 3.65 (m, 4H), 1.35 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06417185B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-b634127504ca40c3b7ae2f51dc4c5d4b |
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| Source note | uspto-grants-2002_07 |
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