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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046197Generated: November 1, 2026

2-Bromo-5-fluoropyridine → HCID 44625911, compound

https://huagongshe.com/reaction/1046197

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-5-fluoropyridineHCID 2783171—
Reactant(S)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-3-((S)-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)-1,3-oxazinan-2-oneHCID 59532385—
SolventEthyl AcetateHCID 8857—
ProductHCID 44625911HCID 44625911—

Reaction Steps

The title compound was prepared from (S)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-3-((S)-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)-1,3-oxazinan-2-one and 2-bromo-5-fluoropyridine following a procedure analogous to that described in Example 1 Step 2. LC-MS Method 2 tR=1.363, m/z=390.9; 1H NMR (CDCl3) 1.11 (s, 3H), 1.19 (s, 3H), 1.53 (d, 3H), 2.16-2.30 (m, 4H), 2.32-2.43 (m, 1H), 2.86 (m, 1H), 5.71 (m, 1H), 7.03 (d, 2H), 7.30 (m, 1H), 7.36 (m, 4H), 7.44 (m, 1H), 7.69 (dd, 1H), 7.68 (d, 2H), 8.43 (d, 1H). The compound was dissolved in refluxing ethyl acetate and allowed to cool slowly to rt to afford a solid with mp 159-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569292B2
Source datasetuspto-grants-2013_10
ORD IDord-9076e5ffcf95464f9b3c7c32f148f711
Source noteuspto-grants-2013_10