HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795457Generated: November 1, 2026
1-Phenethylamine, (-)- → HCID 21023644, compound
https://huagongshe.com/reaction/1795457
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Phenethylamine, (-)- | HCID 75818 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | HCID 22185182 | HCID 22185182 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21023644 | HCID 21023644 | — |
Reaction Steps
To a 100 mL RBF, was added 6-(2-chloro-pyridin-4-yl)-2-(2-methoxymethyl-pyrrolidin-1-yl)-3-methyl-5-m-tolyl-3H-pyrimidin-4-one (0.3 g, 0.71 mmol), 50 mL toluene, and (S)-α-methyl benzylamine (0.181 mL, 1.42 mmol). The mixture was degassed by nitrogen bubbled through for 1 h. After added Pd(OAc)2 (24 mg, 0.106 mmol), BINAP (65 mg, 0.106 mmol) and NaOtBu (0.191 g, 2.0 mmol), the mixture was warmed up to 100° C. and stirred for 3 h under nitrogen. The mixture was cooled down to rt, and vacuumed down all volatile composites. After purified by flash chromatography, the title compound was obtained in 0.18 g as pale yellow solid. MS (ES+): 510 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07026326B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-13c64723dd274cc480c7f4b252274686 |
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| Source note | uspto-grants-2006_04 |
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