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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884367Generated: October 29, 2026

Triethylamine → HCID 58109254, compound

https://huagongshe.com/reaction/884367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Bromo-5-(trifluoromethyl)pyridineHCID 2736434—
ReactantHCID 58109622HCID 58109622—
SolventAcetonitrileHCID 6342—
ProductHCID 58109254HCID 581092547%

Reaction Steps

A mixture of (R)-6-(4-fluorophenyl)-6-(3-hydroxypropyl)-3-((S)-piperidin-3-yl)-1,3-oxazinan-2-one (100 mg, 0.30 mmol), 2-bromo-5-(trifluoromethyl)pyridine (67 mg, 0.36 mmol), and triethylamine (91 mg, 0.90 mmol) in acetonitrile was heated to reflux for 3 h. The reaction mixture was concentrated. The residue was purified by preparative TLC and preparative HPLC to afford (R)-6-(4-fluorophenyl)-6-(3-hydroxypropyl)-3-((S)-1-(5-(trifluoromethyl)pyridin-2-yl) piperidin-3-yl)-1,3-oxazinan-2-one (10.09 mg, 7%). LC-MS Method 2 tR=1.34 min, m/z=482. 1H NMR (400MHz, CDCl3): 1.28 (m, 1H), 1.64 (m, 2H), 1.76 (m, 3H), 1.92 (m, 2H), 2.18 (m, 1H), 2.27 (m, 1H), 2.77 (m, 3H), 3.21 (m, 1H), 3.52 (t, 2H), 3.83 (broad, 1H), 4.11 (d, 1H), 4.25 (d, 1H), 6.57 (d, 1H), 7.03 (t, 2H), 7.23 (m, 2H), 7.54 (d, 1H), 8.29 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242111B2
Source datasetuspto-grants-2012_08
ORD IDord-3635442cdeff496ba86996076e3bbf3c
Source noteuspto-grants-2012_08