Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Reactant | HCID 178429454 | HCID 178429454 | — |
| Product | HCID 178464160 | HCID 178464160 | 68% |
Reaction Steps
In a 100 mL round bottom flask, diethylamine (0.31 mL, 3.0 mmol) was added into the solution of MeMgBr (0.90 mL, 3 mmol) in THF (20 mL). The resulting mixture was stirred at 40° C. for 1 hour, followed by addition of 3-chloro-2-{[(4-hydroxy-6-methylpyrimidin-2-yl)sulfanyl]methyl}benzonitrile (292 mg, 1.0 mmol). After another 1.5 hours, the solvent was removed under vacuum. The crude product was purified by CombiFlash (0 to 20% MeOH in DCM) to provide the title compound as a grey-yellow solid (200 mg, 68% yield); 1H NMR (400 MHz, DMSO-d6): δ 1.17 (t, 6H), 2.28 (s, 3H), 3.31 (q, 4H), 4.60-4.80 (m, 2H), 6.03 (br, 1H), 7.57 (m, 2H), 7.88 (d, 1H); M+365.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315521B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-70d970dab3614f9fa470fab43e32e66b |
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| Source note | uspto-grants-2016_04 |
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