HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095454Generated: November 2, 2026
3-bromo-5-[[1-(tert-butoxycarbonyl)-2(R)-pyrrolidinyl]methoxy]pyridine → HCID 59371470, compound
https://huagongshe.com/reaction/2095454
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-bromo-5-[[1-(tert-butoxycarbonyl)-2(R)-pyrrolidinyl]methoxy]pyridine | HCID 15480236 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 56829989 | HCID 56829989 | — |
| Catalyst | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59371470 | HCID 59371470 | 64% |
Reaction Steps
To a solution of 3-bromo-5-[[1-(tert-butoxycarbonyl)-2(R)-pyrrolidinyl]methoxy]pyridine (254 mg, 0.71 mmol) and 4-[2-(4-methylbenzyloxy)ethyl]piperidine (182 mg, 0.78 mmol, 1.1 equiv.) in anhydrous toluene (2 mL) were added successively sodium tert-butoxide (102 mg, 1.07 mmol), tris(dibenzylideneacetone)dipalladium(0) (13.0 mg, 14 μmol, 0.02 equiv.), and 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (Xantphos; 24.7 mg, 43 μmol, 0.06 equiv.). The mixture was degassed and purged with Ar (3 cycles), then warmed to 98-100° C. for 4 h. After cooling to room temperature, the mixture was diluted with EtOAc, and the solution was washed with brine, dried over Na2SO4, and evaporated. The residue was purified by CC on SiO2 with CH2Cl2/EtOAc 4:1, then 1:1. The product (231 mg, 64%) was obtained as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445684B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-89d9d99b171b42bb886955a3a0a617b0 |
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| Source note | uspto-grants-2013_05 |
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