Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (-)-Epichlorohydrin | HCID 2734062 | — |
| Reactant | HCID 136339878 | HCID 136339878 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86645307 | HCID 86645307 | 109.6% |
Reaction Steps
To a solution of 4-[5-(2-diethylamino-6-methyl-pyrimidin-4-yl)-[1,2,4]oxadiazol-3-yl]-2-ethyl-6-methyl-phenol (700 mg, 1.90 mmol) in isopropanol (12 mL), are added 3M aq. NaOH (4 mL) and R-epichlorohydrine (1.49 mL, 19.0 mmol). The reaction mixture is stirred at rt for 15 h, then is diluted with EtOAc and washed with 1M aq. NaOH followed by brine. The org. phase is dried over Na2SO4, filtered, evaporated and purified by CC (eluting with Heptane/EtOAc 4:1) to give the title compound as a yellow oil (882 mg); LC-MS: tR=1.23; [M+H]+=424.04. 1H NMR (CDCl3) δ 1.25 (t, J=7.0 Hz, 6H), 1.33 (t, J=7.5 Hz, 3H), 2.41 (s, 3H), 2.47 (s, 3H), 2.79 (m, 3H), 2.94 (t, J=4.5 Hz, 1H), 3.42 (m, 1H), 3.76 (q, J=7.0 Hz, 4H), 3.83 (dd, J=11.0, 5.8 Hz, 1H), 4.13 (dd, J=11.0, 3.0 Hz, 1H), 7.23 (s, 1H), 7.89 (d, J=5.5 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299086B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-a737585777d74859add0215c0cb61f63 |
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| Source note | uspto-grants-2012_10 |
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