HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555802Generated: October 26, 2026
Lithium Hexamethyldisilazide → [4-(3-Chloro-pyrazin-2-yloxy)-phenyl]-(6-fluoro-1H-benzoimidazol-2-YL)-methanone
https://huagongshe.com/reaction/555802
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Ethyl 4-[(3-chloropyrazin-2-yl)oxy]benzoate | HCID 45031059 | — |
| Reactant | 6-Fluoro benzoimidazole-1-carboxylic acid tert-butyl ester | HCID 59351372 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [4-(3-Chloro-pyrazin-2-yloxy)-phenyl]-(6-fluoro-1H-benzoimidazol-2-YL)-methanone | HCID 46207941 | — |
Reaction Steps
A solution of 4-(3-Chloro-pyrazin-2-yloxy)-benzoic acid ethyl ester (20 g, 84.7 mmol) and 6-fluoro benzoimidazole-1-carboxylic acid tert-butyl ester (21.2 g, 76.3 mmol) in freshly dried THF (150 mL) was cooled to −78° C. LiHMDS (106 mL, 106 mmol) was added slowly to it over 1.2 h. The reaction mixture was stirred at the same temperature for 3.5 h. The reaction was brought to −20° C. and slowly quenched with addition of 2N HCl until pH 3-4. The resulting mixture was stirred at RT for 1 h, extracted with ethyl acetate (3×200 mL), and washed with water (2×100 mL). The organic layer was dried (Na2SO4) and concentrated. To the crude product was added methanol (70 mL). After stirring for 1 h, the solid was collected by filtration to give the title compound. MS (ESI, pos. ion) m/z: 369.2 (M+1). IC50 (uM) +.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08053438B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-140bcf612f294b988fae8d1ab3ea1277 |
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| Source note | uspto-grants-2011_11 |
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