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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187485Generated: October 30, 2026

1,1'-Carbonyldiimidazole → AR-A000002

https://huagongshe.com/reaction/2187485

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-(Morpholin-4-yl)benzoic acidHCID 345278—
Reactant(2R)-5-Methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthalen-2-amineHCID 53918832—
SolventDimethylformamideHCID 6228—
ProductAmmoniaHCID 222—
ProductAR-A000002HCID 9846516146.9%

Reaction Conditions

Temperature75 °C

Reaction Steps

4-Morpholinobenzoic acid (92 mg, 0.44 mmol) was dissolved in dry N,N-dimethylformamide (2 mL) and flushed with nitrogen. To the solution was added 1,1′-carbonyldiimidazole (76 mg, 0.47 mmol) and the reaction mixture was stirred at 75° C. for 1.5 h. The solution was cooled to room temperature and (R)-2-amino-5-methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthalene (110 mg, 0.42 mmol), dissolved in dry N,N-dimethylformamide (2 mL) was added. The solution was stirred at room temperature for 30 h. The solvent was evaporated in vacuo giving 290 mg of a crude product. Purification by preparative TLC on silica gel using chloroform/methanol/conc. NH3 (95:5:0.5) as the eluent afforded 145 mg (73% yield) of the title compound as a white solid: mp >231° C. (dec); EIMS (70 eV) m/z (relative intensity) 448 (3, M+); [α]21D−60° (c 0.15, chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410532B1
Source datasetuspto-grants-2002_06
ORD IDord-2040669338fc40bf9f36a76e4e978d9f
Source noteuspto-grants-2002_06