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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103286Generated: October 30, 2026

3-Butyl-8-azabicyclo[3,2,1]octane → HCID 68913194, compound

https://huagongshe.com/reaction/2103286

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Butyl-8-azabicyclo[3,2,1]octaneHCID 68907966—
ReactantHCID 68910871HCID 68910871—
SolventAcetonitrileHCID 6342—
ProductHCID 68913194HCID 6891319430.5%

Reaction Steps

A 4 mL vial was charged with (S)-1-(3-iodo-2-methylpropyl)-3,4-dihydro-1H-quinolin-2-one (122LH18) (0.185 g, 0.56 mmol) and 3-butyl-8-azabicyclo[3.2.1]octane (0.100 g, 0.60 mmol) in MeCN (0.5 mL) and shaken at 40° for 20 h. The reaction mixture was quenched with water, basified with ammonium hydroxide, and the product extracted into EtOAc. The combined organic layers were dried over Na2SO4, filtered, and concentrated. The product was purified by flash CC (SiO2; n-heptane/EtOAc 4:1) to give the title compound (107LH54) (0.063 g, 30%). 1H NMR (CD3OD) δ 7.29-7.19 (m, 3H), 7.03-6.99 (m, 1H), 4.03-4.00 (m, 2H), 3.14-3.13 (m, 1H), 3.07-3.05 (m, 1H), 2.90-2.86 (m, 2H), 2.62-2.57 (m, 2H), 2.28-2.19 (m, 2H), 1.97-1.82 (m, 3), 1.58-1.42 (m, 5H), 1.34-1.15 (m, 8H), 0.90-0.87 (m, 6H); 13C NMR (CD3OD) δ 173.1, 140.3, 129.1, 128.4, 128.3, 124.3, 117.2, 62.2, 61.2, 58.2, 46.5, 39.0, 38.0, 32.9, 32.1, 30.3, 29.1, 27.8, 27.3, 26.3, 24.0, 17.1, 14.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576100B2
Source datasetuspto-grants-2009_08
ORD IDord-ff3085f3d25c410881bb561a3598140b
Source noteuspto-grants-2009_08