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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409982Generated: October 30, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 86703296, compound

https://huagongshe.com/reaction/2409982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant6-Bromopyridine-2-carbaldehydeHCID 2757009—
Reactant6-methoxy-2-phenyl-1H-indoleHCID 10751571—
SolventDichloromethaneHCID 6344—
ProductHCID 86703296HCID 8670329687.4%

Reaction Steps

To a suspension of 6-methoxy-2-phenyl-1H-indole (893 mg) and 6-bromopyridine-2-carboaldehyde (744 mg) in dichloromethane (13.3 mL) was added 1,8-diazabicyclo[5,4,0]-7-undecene (0.060 mL), and the mixture was stirred at room temperature for 13 hours under an argon atmosphere. The reaction mixture was purified by aminopropylated silica gel column chromatography (eluting solvent: ethyl acetate-hexane) to obtain the title compound (1.43 g). 1H-NMR (CDCl3) δ ppm: 3.81 (3H, s), 4.71 (1H, d, J=2.6 Hz), 6.09 (1H, d, J=2.6 Hz), 6.65 (1H, dd, J=2.3, 8.7 Hz), 6.86 (1H, d, J=2.3 Hz), 7.02-7.13 (2H, m), 7.33-7.54 (5H, m), 7.64-7.72 (2H, m), 8.10 (1H, br s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815903B2
Source datasetuspto-grants-2014_08
ORD IDord-4d192f37bb56421982ce9a9a54c9813a
Source noteuspto-grants-2014_08