HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bromide → HCID 13530093, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | 5-Chloropyrimidin-2-ol hydrochloride | HCID 12648523 | — |
| Reactant | 1-[(Chloromethyl)sulfanyl]-4-fluorobenzene | HCID 20161342 | — |
| Reactant | HCID 22648495 | HCID 22648495 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13530093 | HCID 13530093 | — |
Reaction Steps
The title compound was prepared from 5-chloropyrimidin-2-one hydrochloride (10 mmol) and 4-fluoro-1(chloromethylthio)benzene (10 mmol) in a manner similar to that described in Example 2. The reaction time was 21/2h. Yield: 1.60 g (59%) of the N- and O-isomers in the ratio 2:1. The N-isomer was isolated by its lower solubility in methanol; m.p. 179° C. (MeOH/H2O/isoPrOH). 1H NMR (DMSO/d6): δ 5.25 (CH2), 6.9-7.7 (Ph), 8.07 and 8.53 (H-4 and H-6, J 4 Hz). IR (KBr): 1660 cm-1 (CO). (Found: C49.80; H2.54. Calc. for C11H8ClFN2OS: C48.81; H2.98). MS [70 eV, m/z (% rel. int.]): 270/272 (4/2,M), 143/145 (100/32).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04705791 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-9a0dcb3a48634d34902b8753bd7099a8 |
| Source note | uspto-grants-1987_11 |