HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205550Generated: November 1, 2026
HCID 86680497, compound → HCID 71544070, compound
https://huagongshe.com/reaction/2205550
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86680497 | HCID 86680497 | — |
| Reactant | HCID 178418365 | HCID 178418365 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 71544070 | HCID 71544070 | 20% |
Reaction Steps
To a stirred solution of (2-(4-fluorophenyl)thiazol-5-yl)(pyridin-4-yl)methanone (0.1 g, 0.352 mmol) in THF (10 mL) was added isopropyl magnesium bromide (0.1 g, 0.704 mmol) at 0° C. The reaction mixture was stirred for 1 hour at room temperature. After completion of the reaction, the reaction mixture was quenched with ammonium chloride (5 mL) at 0° C., extracted with ethyl acetate (2×20 mL), washed with water followed by brine (20 mL), dried over Na2SO4, and concentrated under reduced pressure. The crude was purifying by the preparative TLC (Mobile phase: 10% MeOH in DCM) to obtain pure 1-(2-(4-fluorophenyl)thiazol-5-yl)-2-methyl-1-(pyridin-4-yl)propan-1-ol (0.023 g, 20% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.52 (d, 2H), 7.92 (t, 3H), 7.56 (d, 2H), 7.27 (t, 2H), 6.22 (s, 1H), 2.79 (t, 1H), 0.98 (d, 3H), 0.71 (d, 3H); LC-MS m/z calculated for [M+H]+329.10. found 329.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09371316B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-ce5fc5ba847c4e399e593be20be0e126 |
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| Source note | uspto-grants-2016_06 |
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