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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880617Generated: November 4, 2026

1,1'-Carbonyldiimidazole → HCID 25138378, compound

https://huagongshe.com/reaction/1880617

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(2E)-3-[6-(Trifluoromethyl)pyridin-3-yl]prop-2-enoic acidHCID 5709645—
Reactant5,8-Dichloro-1,2,3,4-tetrahydroisoquinoline-6,7-diol--hydrogen bromide (1/1)HCID 68508172—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 25138378HCID 2513837855%

Reaction Steps

To a solution of CDI (83 mg, 0.51 mmol) in EtOAc (2 mL) was added (E)-3-(6-(trifluoromethyl)pyridin-3-yl)acrylic acid (100 mg, 0.46 mmol). The resulting mixture was heated at reflux for 1 h after which HOBt (35 mg, 0.23 mmol) and 5,8-dichloro-1,2,3,4-tetrahydroisoquinoline-6,7-diol hydro bromide (145 mg, 0.46 mmol) were added. Heating at reflux was continued for 3 h before the reaction mixture was allowed to cool to rt. It was then poured into water (15 mL) and the water-phase was extracted with EtOAc (3×15 mL). Combined organics were washed with water (10 mL) and brine (10 mL) and dried (MgSO4). After filtration and evaporation, the crude was purified by column chromatography (SiO2, EtOAc:petroleum ether 50:50) to give a bright yellow solid which was purified further by precipitating the product in EtOAc via addition of petroleum ether. After decantation of the solvent and drying, the title compound (110 mg, 0.25 mmol, 55%) was obtained as a light reddish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318768B2
Source datasetuspto-grants-2012_11
ORD IDord-eaf145bd000042eda80fcef18018cfc6
Source noteuspto-grants-2012_11