HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629810Generated: November 2, 2026
4-Methoxypiperidine → HCID 117602079, compound
https://huagongshe.com/reaction/629810
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methoxypiperidine | HCID 77666 | — |
| Reactant | 5-Bromoisoquinoline | HCID 736487 | — |
| Reactant | sodium 2-methylpropan-2-olate | HCID 178418730 | — |
| Catalyst | Binap, (A+-)- | HCID 634876 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | HCID 117602079 | HCID 117602079 | 52.4% |
Reaction Steps
To 5-bromoisoquinoline (10.40 g, 50 mmol), 4-methoxypiperidine (4.92 mL, 50.0 mmol), Pd2(dba)3 (0.458 g, 0.500 mmol), BINAP (0.934 g, 1.500 mmol), and t-BuONa (6.73 g, 70.0 mmol) was added degassed toluene (60 mL) and the reaction was heated under N2 to 85° C. for 24 h and then to 105° C. for 3 h. The reaction mixture was cooled to ambient temperature and water was added. The phases were separated and the aqueous layer extracted three times with ethyl acetate. The combined organics were washed with brine, dried (Na2SO4), filtered and purified by silica gel chromatography to afford 6.34 g (52.4%) of Intermediate 3A as a pale yellow solid. MS (ESI) m/z: 243.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315519B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-726ee1b1c78c474c84c7864fb8b65df1 |
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| Source note | uspto-grants-2016_04 |
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