HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361692Generated: October 30, 2026
Tetrahydrofuran → (2-Methoxy-phenyl)-{4-methyl-3-[3-(2-methylamino-pyrimidin-4-yl)-pyridin-2-yloxy]-phenyl}-methanone
https://huagongshe.com/reaction/1361692
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Magnesium Bromide | HCID 82241 | — |
| Reactant | HCID 66970597 | HCID 66970597 | — |
| Reactant | 4-Methyl-3-[3-(2-methylamino-pyrimidin-4-yl)-pyridin-2-yloxy]-benzoyl chloride | HCID 86602596 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2-Methoxy-phenyl)-{4-methyl-3-[3-(2-methylamino-pyrimidin-4-yl)-pyridin-2-yloxy]-phenyl}-methanone | HCID 58588533 | — |
Reaction Steps
To 4-methyl-3-[3-(2-methylamino-pyrimidin-4-yl)-pyridin-2-yloxy]-benzoyl chloride (50 mg, 0.14 mmol) in a flame dried, round-bottom flask under nitrogen and cooled to −78° C. was added 4 ml of THF, 2 ml methylene chloride and magnesium-bromide-2-methoxy-benzene in THF (0.3 ml, 0.6 mmol). After addition of the magnesium-bromide, the −78° C. dry ice bath was removed and the reaction allowed to warm to room temperature over 4 h. The reaction was quenched with saturated sodium bicarbonate solution and extracted with methylene chloride and brine. The organic layers were combined, dried with sodium sulfate and filtered. The solvent was removed under vacuum and the product was purified via preparative HPLC (Gilson). MS m/z=427 [M+H]+. Calc'd for C25H22N4O3: 426.48.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07880000B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-837b50f92f14484296ee7f515cc2bff0 |
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| Source note | uspto-grants-2011_02 |
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