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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258078Generated: October 25, 2026

1,1'-Carbonyldiimidazole → NGB 2904 hydrochloride

https://huagongshe.com/reaction/2258078

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 (185 mg, 78%). Hydrochloride salt was prepared lay treating the free base with a solution of hydrogen chloride in ethyl acetate (top 262-4° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05659033
Source datasetuspto-grants-1997_08
ORD IDord-385f0161e99f4bf781a4ae6f4f2e7f7f
Source noteuspto-grants-1997_08