HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971600Generated: October 31, 2026
N-(2-(p-bromophenoxy)ethyl)pyrrolidine → HCID 59276591, compound
https://huagongshe.com/reaction/1971600
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-(2-(p-bromophenoxy)ethyl)pyrrolidine | HCID 70657 | — |
| Reactant | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 59589689 | HCID 59589689 | — |
| Catalyst | Dimethylacetamide | HCID 31374 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59276591 | HCID 59276591 | — |
Reaction Steps
In a microwave vial, N*5*-cyclopentyl-[1,2,4]triazolo[1,5-a]pyridine-2,5-diamine (0.07 g, 0.322 mmol), 1-(2-(4-bromophenoxy)ethyl)pyrrolidine (0.13 g, 0.483 mmol), bis(dibenzylideneacetone)palladium (0.01 g, 0.016 mmol), xantphos (0.019 g, 0.032 mmol) and sodium tert-butoxide (0.063 g, 0.644 mmol) were added successively. 1,4-Dioxane (1.2 mL) and dimethylacetamide (4 drops) were added and the vial was sealed and heated under microwave irradiation (1500° C., 10 min). The mixture was filtered and purified by preparatory HPLC. LCMS Method: 2: RT: 2.51 min, MI: 407 [M+1]. NMR 1H (DMSO): 1.55-1.75 (m, 10H), 2.03-2.08 (m, 2H), 2.55-2.65 (m, 4H), 2.84 (t, 2H), 3.93-4.00 (m, 1H), 4.01 (t, 2H), 6.10 (d, 1H), 6.15 (d, 1H), 6.69 (d, 1H), 6.87 (d, 2H), 7.37 (t, 1H), 7.63 (d, 2H), 9.17 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431596B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-c9bb3a5972eb49a1a96bdf427c7b840a |
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| Source note | uspto-grants-2013_04 |
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