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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509150Generated: October 30, 2026

Hydrogen Bromide → HCID 123471154, compound

https://huagongshe.com/reaction/1509150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium hydrideHCID 24758—
Reactant3-(Bromomethyl)pyridineHCID 245934—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67256382HCID 67256382—
SolventDimethylformamideHCID 6228—
ProductHCID 123471154HCID 12347115438%

Reaction Steps

To a solution of tert-butyl(1-(4-(2-oxo-7-phenyl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-6-yl)phenyl)cyclobutyl)carbamate (51 mg, 0.11 mmol) in dry DMF (1 ml) was added sodium hydride (11 mg, 0.26 mmol) and 3-(bromomethyl)pyridine.HBr (33 mg, 0.13 mmol) under nitrogen. The resulting mixture was stirred for 1 hour at room temperature. A saturated solution of NaHCO3 was added and the mixture was extracted with dichloromethane (3×10 ml) using a phase separator (Isolute® SPE). The combined organic phases were concentrated to dryness under reduced pressure. The resulting residue was purified by Biotage silica gel chromatography (gradient 0 to 80% EtOAc in cyclohexane) to give the title compound (23 mg, 38%). 1H NMR (500 MHz, CDCl3): 8.60-8.50 (2H, br s), 7.60 (2H, d), 7.28 (1H, s), 7.19-7.15 (6H, m), 7.12 (1H, s), 6.97 (2H, d), 5.13 (2H, s), 4.93 (3H, s), 2.52-2.20 (4H, m), 2.00-1.95 (1H, m), 1.75-1.70 (1H, m), 1.44-1.15 (9H, br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-2f7fb7ab4e454f4f8c3686b674044608
Source noteuspto-grants-2015_12