HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103287Generated: October 30, 2026
3-Pentyl-8-azabicyclo[3.2.1]octane → HCID 68912293, compound
https://huagongshe.com/reaction/2103287
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Pentyl-8-azabicyclo[3.2.1]octane | HCID 21989852 | — |
| Reactant | HCID 68910871 | HCID 68910871 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68912293 | HCID 68912293 | 35% |
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-pentyl-8-azabicyclo[3.2.1]octane (0.112 g, 0.62 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 (107LH55) (0.075 g, 35%). 1H NMR (CD3OD) δ 7.28-7.18 (m, 3H), 7.01 (t, J-=7.2 Hz, 1H), 4.03 (d, J=7.0 Hz, 2H), 3.11-3.04 (m, 2H), 2.90-2.85 (m, 2), 2.64-2.56 (m 2H), 2.28-2.11 (m, 4H), 1.97-1.84 (m, 3H), 1.66-1.54 (m, 3H), 1.42-1.21 (m, 10H), 0.90-0.85 (m, 2 CH3); 13C NMR (CD3OD) δ 173.1, 140.3, 129.1, 128.4, 128.3, 124.3, 117.1, 61.4, 60.2, 58.3, 46.4, 39.5, 37.1, 37.0, 33.1, 32.9, 32.2, 29.5, 29.4, 28.5, 27.9, 26.3, 23.7, 17.1, 14.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576100B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-df15b549fe074f5089a714168535d333 |
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| Source note | uspto-grants-2009_08 |
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