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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102652Generated: October 30, 2026

Sodium Iodide → HCID 10125819, compound

https://huagongshe.com/reaction/2102652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant4-ButylpiperidineHCID 13283867—
Reactant4-(3-chloropropyl)-2H-1,4-benzoxazin-3(4H)-oneHCID 23345150—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductHCID 10125819HCID 10125819—

Reaction Conditions

Temperature60 °C

Reaction Steps

NaI (1.33 g, 8.87 mmol), K2CO3 (1.23 g, 8.90 mmol), and 4-butylpiperidine (0.66 g, 4.71 mmol) in acetonitrile (10 mL) were stirred at rt. 4-(3-chloropropyl)-4H-benzo[1,4]oxazin-3-one (1.0 g, 4.43 mmol) in acetonitrile (15 mL) was added via a syringe. The reaction was stirred at 60° C. for 13 hours and then at 80° C. for another 5 hours under nitrogen atmosphere and concentrated in vacuo. Water (150 mL) was added and the reaction mixture was extracted with ethyl acetate (3×150 mL). The combined organic phases were dried (Na2SO4) and concentrated in vacuo to give 1.58 g of crude. The crude product was subjected to CC[eluent:EtOAC:MeOH(100:1-5%)] to give the pure title compound. Yield 0.82 g 56.0% HPLC-MS [M+H]+ 331 (UV/MS(%)=100/99. 1H NMR (CDCl3): δ 0.88 (t, 3H), 1.21 (m, 6H), 1.26 (m, 3H), 1.66 (d, 2H), 1.86 (m, 4H), 2.37 (t, 2H), 2.86, (d, 2H), 3.97 (t, 2H), 4.58 (s, 2H), 6.99 (m, 3H), 7.11 (d, 1H), 13C NMR (CDCl3): δ 14.22, 23.04, 24.90, 29.17, 32.68, 35.95, 36.46, 39.74, 54.31, 56.02, 67.77, 115.26, 117.15, 122.83, 123.83, 128.78, 145.50, 164.34.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576078B2
Source datasetuspto-grants-2009_08
ORD IDord-09b9f2fa505b4c7a9e463e6cc0f88514
Source noteuspto-grants-2009_08