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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175358Generated: October 27, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 2-[-2-(5,8-Dimethyl[1,2,4]triazolo[1,5-a]pyrazin-2-yl)-vinyl]-5H-imidazo[2,1-a]isoindole

https://huagongshe.com/reaction/2175358

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant5H-Imidazo[2,1-a]isoindole-2-carbaldehydeHCID 22224534—
Reactant((5,8-Dimethyl-[1,2,4]triazolo[1,5-a]pyrazin-2-yl)methyl)triphenylphosphonium chlorideHCID 86665503—
SolventTetrahydrofuranHCID 8028—
Product2-[-2-(5,8-Dimethyl[1,2,4]triazolo[1,5-a]pyrazin-2-yl)-vinyl]-5H-imidazo[2,1-a]isoindoleHCID 69670867—

Reaction Steps

A solution of 5H-imidazo[2,1-a]isoindole-2-carbaldehyde (150 mg, 0.81 mmol) in dry THF (5.3 mL) was added to (5,8-Dimethyl-[1,2,4]triazolo[1,5-a]pyrazin-2-ylmethyl)-triphenyl-phosphonium chloride (374 mg, 0.81 mmol) under argon and 1,8-diazabicyclo [5,4,0]undec-7-ene (120 micro L, 0.81 mmol) was added. The reaction mixture was stirred at room temperature for 12 hours after which it was evaporated onto silica gel (2 g). Silica gel chromatography (gradient elution, A:B 100:0 to 0:100, where A is ethyl acetate and B is 10% MeOH in ethyl acetate) afforded the title compound as a mixture of the cis and trans isomers (139 mg, 52%) LC-MS: m/z=329.3 (MH+), tR=0.96 minutes

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062060B2
Source datasetuspto-grants-2015_06
ORD IDord-10c7df8afdb44b1baf578eba315784b2
Source noteuspto-grants-2015_06