HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504344Generated: October 31, 2026
2-Methyltetrahydrofuran → HCID 178461449, compound
https://huagongshe.com/reaction/1504344
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 89541653 | HCID 89541653 | — |
| Reactant | HCID 178461444 | HCID 178461444 | — |
| Catalyst | Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) | HCID 11714597 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178461449 | HCID 178461449 | 93% |
Reaction Steps
To a round bottom flask was added (2S,4S)-tert-butyl 2-(4-(4-bromophenyl)-1H-imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate (10 g, 24.61 mmol), (R)-(5-chloro-4-(6-(2-methyl-4-pivaloylpiperazin-1-yl)nicotinamido)-2-(trifluoromethoxy)phenyl)boronic acid (14.16 g, 26.1 mmol), sodium bicarbonate (7.24 g, 86 mmol), bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) (0.17 g, 0.246 mmol), 2 methyltetrahydrofuran (120 mL) and water (44.3 mL) to give a suspension. The reaction mixture was degassed with nitrogen for 10 min then heated at 70° C. overnight. Water (60 mL) was added and the layers were separated. The organic layer was washed with brine, dried over Na2SO4, and evaporated to give crude product (27.3 g). The crude product was purified by flash chromatography (300 g silica gel, 20-100% EtOAc (50 min), then 100% EtOAc (20 min)) to give the title intermediate (18.8 g; 93% yield) HPLC Method B: Retention time 14.99 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212168B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-d7b396af3a1e4a89bb7a53339b9d8bb1 |
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| Source note | uspto-grants-2015_12 |
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