Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thymine | HCID 1135 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N3-benzoylthymine | HCID 10933275 | — |
Reaction Steps
To a solution of thymine (1) in THF was added pyridine and the reaction was cooled to 0° C. Benzoyl chloride was added carefully at 0° C. and the reaction was stirred overnight at room temperature. The reaction mass was evaporated to give the crude solid which was purified by SiO2 flash chromatography to give the N3-benzoyl thymine (4) as a white solid. NMR (600 MHz, CD3OD): δ 7.94 (m, 2H), 7.71 (t, 1H, J=7.3 Hz), 7.57 (m, 2H), 7.38 (s, 1H), 1.90 (s, 3H); Mass (ESI-MS): 231.22 (M+H); m.p: 178-180° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403778B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-26215334e2f64badafdba3b74534587f |
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| Source note | uspto-grants-2016_08 |
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