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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350175Generated: November 1, 2026

Potassium Carbonate → HCID 21094414, compound

https://huagongshe.com/reaction/1350175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 69319657HCID 69319657—
SolventDimethylformamideHCID 6228—
ProductHCID 21094414HCID 21094414171.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

This compound was prepared by treatment of (3R)-3-ethyl-3,4-dihydro-8-isopropoxy-10-(trifluoromethyl)-2H-[1,4]oxazino[2,3-f]quinoline (20 mg, 0.059 mmol), 2-methallyl bromide (40 mg, 0.30 mmol) and K2CO3 (41 mg, 0.30 mmol) in 1 mL DMF heated at 50° C. for 16 h. The reaction was treated with an additional 2-methallyl bromide (60 mg) and was heated overnight at 50° C. The mixture was extracted with ethyl acetate (2×25 mL), and the combined organic layers were washed with water (25 mL), brine (25 mL), dried over MgSO4, filtered, and concentrated afford 20 mg (87%) of (3R)-3-ethyl-4-(2-methyl-2-propenyl)-3,4-dihydro-8-isopropoxy-10-(trifluoromethyl)-2H-[1,4]oxazino[2,3-f]quinoline after flash chromatography (9:1 hexanes:EtOAc). 1H NMR (400 MHz, CDCl3) δ7.39 (d, J=9.0, 1H), 7.18 (s, 1H), 7.12 (d, J=9.0, 1H), 5.47 (septet, J=6.2, 1H), 4.91 (broad s, 2H), 4.33 (dd, J=10.7, 2.1, 1H), 3.96 (dd, J=10.7, 2.6, 1H), 3.85 (d, AB, J=17.1, 1H), 3.80 (d, AB, J=17.1, 1H), 3.20–3.26 (m, 1H), 1.79 (s, 3H), 1.58–1.68 (m, 2H), 1.38 (d, J=6.2, 3H), 1.37 (d, J=6.2, 3H), 0.96 (t, J=7.4, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214690B2
Source datasetuspto-grants-2007_05
ORD IDord-65b9615eb9d74107af3a430f2fccd060
Source noteuspto-grants-2007_05