Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloromethyl 2-(trimethylsilyl)ethyl ether | HCID 2724271 | — |
| Reactant | 1H-Pyrrolo[2,3-c]pyridine-4-carbonitrile | HCID 46835724 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86689864 | HCID 86689864 | 57.9% |
Reaction Steps
To a solution of 1H-pyrrolo[2,3-c]pyridine-4-carbonitrile (618 mg, 4.32 mmol) in anhydrous THF (30 mL) at 0° C. was slowly added NaH (60% in mineral oil, 346 mg, 8.64 mmol). After stirring at 0° C. for 30 min, (2-(chloromethoxy)ethyl)trimethylsilane (865 mg, 5.19 mmol) was added followed by stirring at RT for 1 h. The reaction mixture was quenched with ice water (50 ml) and extracted with EtOAc (50 mL×3). The combined extracts were dried over (MgSO4) filtered, and concentrated under reduced pressure. The residue was purified by SiO2 chromatography eluting with petroleum ether:EtOAc (3:1) to afford 683 mg (57.9%) of 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-c]pyridine-4-carbonitrile as a yellow solid. MS (ESI): m/z=274.2 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815877B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-b1f2a6c9dc6147019812beeeccf902ea |
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| Source note | uspto-grants-2014_08 |
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