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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103283Generated: October 29, 2026

4-Butylpiperidine → HCID 57824846, compound

https://huagongshe.com/reaction/2103283

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ButylpiperidineHCID 13283867—
ReactantHCID 68910871HCID 68910871—
SolventAcetonitrileHCID 6342—
ProductHCID 57824846HCID 5782484654.3%

Reaction Steps

A 4 mL vial was charged with (S)-1-(3-iodo-2-methylpropyl)-3,4-dihydro-1H-quinolin-2-one (122LH18) (0.329 g, 1.0 mmol) and 4-butylpiperidine (0.283 g, 2.0 mmol) in MeCN (2 mL) and shaken at 60° for 20 h. The reaction mixture was concentrated, and the product purified by flash CC (SiO2; EtOAc, EtOAc/MeOH 4:1) to give the title compound (107LH47-A) (0.186 g, 54%). 1H NMR (CD3OD) δ 7.26-7.19 (M, 3H), 7.04-7.00 (m, 1H), 2.93-2.88 (m, 3H), 2.77 (d, J=10.4 Hz, 2H), 2.62-2.58 (m, 2H), 2.29-2.06 (m, 3H), 1.93-1.86 (m, 2H), 1.68-1.62 (m, 2H), 1.31-1.22 (m, 9H), 0.91-0.86 (m, 2 CH3); 13C NMR (CD3OD) δ 173.2, 140.3, 129.1, 128.5, 128.4, 124.4, 166.9, 64.9, 56.0, 55.6, 37.5, 36.9, 33.4, 33.3, 32.9, 30.1, 30.1, 26.2, 24.0, 17.2, 14.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576100B2
Source datasetuspto-grants-2009_08
ORD IDord-780a1545164d42b9803b5d6c091cdb6a
Source noteuspto-grants-2009_08