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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187442Generated: October 30, 2026

Carbon Dioxide → HCID 54551314, compound

https://huagongshe.com/reaction/2187442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-(1H-pyrrol-1-yl)benzoic acidHCID 728521—
Reactant(R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthaleneHCID 53960413—
SolventDimethylformamideHCID 6228—
ProductHCID 54551314HCID 5455131462%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of 4-(1H-pyrrol-1-ylbenzoic acid (96 mg, 0.51 mmol) in anhydrous N,N-dimethylformamide (25 mL) was added 1,1′-carbonyldiimidazole (87 mg, 0.54 mmol) and the reaction was heated at 75° C. When the carbon dioxide evolution had ceased (after 30 min), the reaction was cooled to room temperature and a solution of (R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthalene (120 mg, 0.49 mmol) in anhydrous N,N-dimethylformamide (5 mL) was added. The reaction was allowed to stir at ambient temperature for 17 h and the solvent was evaporated in vacuo. Purification on a silica gel column using chloroform/ethanol saturated with NH3 (100:3) as the eluent gave 128 mg (62% yield) of the title compound as white crystals: mp 245-247° C.; [α]21D −69° (c 1.0, chloroform); EIMS (70 eV) m/z (relative intensity) 414 (15, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410530B1
Source datasetuspto-grants-2002_06
ORD IDord-b095619535fe4f88a63c994520cfdf86
Source noteuspto-grants-2002_06