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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986741Generated: October 26, 2026

Sodium Iodide → 4-[3-(4-Butylpiperidin-1-yl)propyl]-6-methoxy-4H-benzo[1,4]oxazin-3-one

https://huagongshe.com/reaction/1986741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant4-ButylpiperidineHCID 13283867—
Reactant4-(3-Chloropropyl)-6-methoxy-4H-benzo[1,4]oxazin-3-oneHCID 68891997—
SolventEthylacetate heptaneHCID 21899848—
Product4-[3-(4-Butylpiperidin-1-yl)propyl]-6-methoxy-4H-benzo[1,4]oxazin-3-oneHCID 1028695485%

Reaction Steps

4-(3-Chloropropyl)-6-methoxy-4H-benzo[1,4]oxazin-3-one (81MF2249b) (0.127 g, 0.50 mmol), K2CO3 (0.137 g, 1.0 mmol), NaI (0.149 g, 1.0 mmol) and 4-butylpiperidine (0.075 g, 0.52 mmol) were mixed according to GP12. CC (SiO2; Heptane/EtOAc 4:1-4) gave the title compound (81MF2249) (0.14 g, 85%). 1H NMR (CDCl3) d. 6.88 (d, J=8.8 Hz, 1H), 6.67 (d, J=2.4 Hz, 1H), 6.49 (dd, J=8.8 Hz, J=2.4 Hz, 1H), 4.51 (s, 2H), 3.93 (t, 7.2 Hz, 2H), 3.77 (s, 3H), 2.86 (d, J=10.8 Hz, 2H), 2.36 (t, J=7.2 Hz, 2H), 1.90-1.80 (m, 4H), 1.64 (d J=8.8 Hz, 2H), 1.29-1.17 (m, 9H), 0.88 (t, J=6.2 Hz, 3H); 13C NMR (CDCl3) d 168.8, 155.6, 139.6, 129.7, 117.2, 107.2, 102.9, 68.0, 56.1, 56.0, 54.4, 39.9, 36.5, 35.9, 32.6, 29.2, 24.9, 23.0, 14.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550459B2
Source datasetuspto-grants-2009_06
ORD IDord-e7a585a31ab843b6ba8243fad5c5f7c8
Source noteuspto-grants-2009_06