HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105036Generated: October 30, 2026
Methyl iodide → N-((5-ethoxy-2-fluoro-3-isopropoxyphenyl)(4-(1-methyl-1H-pyrazol-4-yl)-1-trityl-1H-imidazol-2-yl)methyl)-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenamine
https://huagongshe.com/reaction/2105036
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-((4-(1H-pyrazol-4-yl)-1-trityl-1H-imidazol-2-yl)(5-ethoxy-2-fluoro-3-isopropoxyphenyl)methyl)-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenamine | HCID 68815685 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-((5-ethoxy-2-fluoro-3-isopropoxyphenyl)(4-(1-methyl-1H-pyrazol-4-yl)-1-trityl-1H-imidazol-2-yl)methyl)-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenamine | HCID 68814350 | 62% |
Reaction Steps
To a solution of Intermediate 237.1 (30 mg, 0.04 mmol) in THF (1 mL) at 0° C. was added NaH (3.16 mg, 0.08 mmol), stirred at 0° C. for 30 min, then MeI was added and the reaction mixture was warmed up to rt over 1 h. The reaction mixture was then partitioned between EtOAc and sat. NH4Cl, the organic layer was dried (Na2SO4), filtered and concentrated. The crude product was purified by flash chromatography (0 to 100% EtOAc/hexanes, gradient) to afford 20 mg (62%) of Intermediate 237.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576098B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-240d32b940be48dfb4ec44ed50fa5ade |
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| Source note | uspto-grants-2009_08 |
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