HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193458Generated: October 29, 2026
2,4-Difluorophenylboronic acid → HCID 59532356, compound
https://huagongshe.com/reaction/2193458
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Difluorophenylboronic acid | HCID 2734334 | — |
| Reactant | HCID 59532383 | HCID 59532383 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59532356 | HCID 59532356 | 26% |
Reaction Steps
To a solution of (S)-3-((S)-1-(4-bromophenyl)propyl)-6-(4-fluorophenyl)-6-(2-hydroxy ethyl)-1,3-oxazinan-2-one (60 mg, 0.14 mmol), 2,4-difluorophenylboronic acid (26 mg, 0.17 mmol) and Pd(PPh3)4 (16 mg, 0.01 mmol) in dioxane (5 mL) was added a solution of CsCO3 (2 M, 1 mL) at 0° C. Then the reaction mixture was refluxed overnight under nitrogen. The reaction mixture was washed with water and then extract with CH2Cl2 twice. The combined organic phases were dried over Na2SO4, filtered and concentrated to give the residue, which was purified by preparative HPLC to afford (S)-3-((S)-1-(2′,4′-difluorobiphenyl-4-yl)propyl)-6-(4-fluorophenyl)-6-(2-hydroxyethyl)-1,3-oxazinan-2-one (17 mg, 26%). 1H NMR (CD3OD): 0.96 (m, 3H), 2.01 (m, 2H), 2.12 (m, 2H), 2.30 (m, 2H), 2.48 (m, 1H), 3.10 (m, 1H), 3.33 (m, 1H), 3.65 (m, 1H), 5.38 (m, 1H), 7.02 (m, 4H), 7.08 (m, 2H), 7.28 (m, 4H), 7.42 (m, 1H). 443-114-3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329897B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-e3a6e4a135364058bc2cc075cf736112 |
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| Source note | uspto-grants-2012_12 |
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