Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Reactant | HCID 67405891 | HCID 67405891 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131734720 | HCID 131734720 | 62.7% |
Reaction Steps
To a solution of 9.60 g (59.8 mmol) 2-chloro-5-hydroxy-3-methylpyrimidin-4(3H)-one in 300 ml DMF was added 20.4 ml (149 mmol) PMBCl, and 48.7 g (149 mmol) Cs2CO3. The reaction mixture was heated to 60° C. for 3 h, cooled to rt, quenched with 200 ml water, extracted with 500 ml EtOAc, dried over Na2SO4, filtered, and concentrated in vacuo. Purification by flash chromatography (330 g silica gel, 3-80% EtOAc:hexane) gave 10 g (60% yield) of 2-chloro-5-[(4-methoxybenzyl)oxy]-3-methylpyrimidin -4(31-1)-one. LCMS [M+H]+=281.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260413B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-94712be06dd642c0a0acd078ec328195 |
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| Source note | uspto-grants-2016_02 |
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