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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584562Generated: October 26, 2026

1,1'-Carbonyldiimidazole → NGB 2904 hydrochloride

https://huagongshe.com/reaction/1584562

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant9H-fluorene-2-carboxylic acidHCID 348591—
Reactant1-Piperazinebutanamine, 4-(2,3-dichlorophenyl)-HCID 11098669—
SolventTetrahydrofuranHCID 8028—
ProductNGB 2904 hydrochlorideHCID 19366304139.4%

Reaction Steps

A mixture of 9H-fluorene-2-carboxylic acid (100 mg, 0.48 mmol) and 1,1'-carbonyldiimidazole (80 mg, 0.5 mmol) in 10 mL of anhydrous tetrahydrofuran was stirred for 8 hours. A solution of 4-[4-(2,3-dichlorophenyl)-1-piperazinyl]-1-aminobutane (150 mg, 0.5 mmol) in 1 mL of tetrahydrofuran was added and the resulting mixture was stirred for 30 minutes. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with aqueous Na2CO3 solution, dried (Na2SO4) and concentrated in vacuo to give the title compound (185mg, 78%). Hydrochloride salt was prepared by treating the free base with a solution of hydrogen chloride in ethyl acetate (mp 262-4° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05932734
Source datasetuspto-grants-1999_08
ORD IDord-7e173299fd9d41c6ada69b9ddff2a82e
Source noteuspto-grants-1999_08