HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2,6-Dichloropyridin-3-yl)methanol → 2-[(2,6-dichloro-3-pyridinyl)methylsulfanyl]-6-methyl-1H-pyrimidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2,6-Dichloropyridin-3-yl)methanol | HCID 12259932 | — |
| Reactant | 3-(Bromomethyl)-2,6-dichloropyridine | HCID 12265394 | — |
| Reactant | HCID 178429541 | HCID 178429541 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-[(2,6-dichloro-3-pyridinyl)methylsulfanyl]-6-methyl-1H-pyrimidin-4-one | HCID 178429433 | 82% |
Reaction Steps
The crude (2,6-dichloropyridin-3-yl)methanol was converted to 3-(bromomethyl)-2,6-dichloropyridine, which was then reacted with 6-methyl-2-sulfanylpyrimidin-4-ol in the presence of triethylamine to provide 2-{[(2,6-dichloropyridin-3-yl)methyl]sulfanyl}-6-methylpyrimidin-4-ol as a white solid (0.822 g, 82% yield); 1H NMR (400 MHz, DMSO-d6): δ 2.15 (s, 3H), 4.36 (s, 2H), 5.95 (bs, 1H), 7.40 (d, J=8.0 Hz, 1H), 8.01 (d, J=8.0 Hz, 1H); M+ 302.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040538B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-2e9c899d76284aa0a4b31c5d983a81b2 |
| Source note | uspto-grants-2015_05 |