HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927618Generated: November 2, 2026
METHYL PHENYL-PIPERAZIN-1-YL-ACETATE → HCID 16665205, compound
https://huagongshe.com/reaction/1927618
Participants
| Role | Name | HCID | Charge |
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| Reactant | METHYL PHENYL-PIPERAZIN-1-YL-ACETATE | HCID 4250546 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 48474221 | HCID 48474221 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 16665205 | HCID 16665205 | 6% |
Reaction Steps
A mixture of phenyl-piperazin-1-yl-acetic acid methyl ester (80 mg, 0.4 mmol), 4-bromo-N-(1-ethyl-propyl)-3-fluoro-benzamide (prepared as described in Example 113, Step A; 150 mg, 0.5 mmol), Pd2(dba)3 (6 mg, 0.007 mmol), X-Phos (3 mg, 0.007 mmol), and NaOtBu (67 mg, 0.9 mmol) in toluene (5 mL) was heated at 100° C. for 18 h. The solids were removed by filtration and the filtrate was concentrated to give an oil, which was purified by PTLC to give a beige solid (9 mg, 6%). MS (ESI): mass calcd. for C25H32FN3O3, 441.54; m/z found, 442.5 [M+H]+. 1H NMR (CDCl3): 7.46-7.43 (m, 4H), 7.38-7.33 (m, 3H), 6.90 (t, J=8.3, 1H), 5.66 (d, J=8.5, 1H), 4.07 (s, 1H), 3.70 (s, 3H), 3.20-3.18 (m, 4H), 2.65-2.63 (m, 4H), 1.68-1.55 (m, 3H), 1.49-1.42 (m, 2H), 0.93 (t, J=7.4, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183239B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-eb1ad8785ec44a18ad40cd2e83741036 |
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| Source note | uspto-grants-2012_05 |
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