HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74538Generated: October 30, 2026
Methyl iodide → HCID 58386683, compound
https://huagongshe.com/reaction/74538
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl 7,7-dimethyl-6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylate | HCID 37818370 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58386683 | HCID 58386683 | — |
Reaction Steps
2.10 g (8.36 mmol) tert. butyl 7,7-dimethyl-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridine-5-carboxylate were placed in 25 mL DMF. While cooling with ice, 350 mg (8.75 mmol) sodium hydride (55%) were added. The reaction mixture was stirred for 30 min, then 0.540 mL (8.67 mmol) iodomethane were added and the mixture was stirred for 1 h at 0° C. The reaction mixture was concentrated to dryness by rotary evaporation and the residue was mixed with water and extracted with EtOAc. The organic phase was dried, filtered and concentrated to dryness by rotary evaporation. The residue was purified by HPLC. The product-containing fractions were combined and organic solvent was eliminated by rotary evaporation. The aqueous residue was extracted with DCM. The organic phase was dried, filtered and concentrated to dryness by rotary evaporation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829006B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-16864c26d23144a79b6ffdda67a79165 |
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| Source note | uspto-grants-2014_09 |
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