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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098341Generated: October 30, 2026

Dabco → HCID 66810931, compound

https://huagongshe.com/reaction/1098341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDabcoHCID 9237—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
ReactantHCID 66811072HCID 66811072—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 66810931HCID 6681093173%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 2-tert-butyl-1H-benzoimidazole-4-carboxylic acid hydrochloride (1.11 g, 4.37 mmol) in anhydrous N,N-dimethylformamide (5 mL) was added 1,1′-carbonyldiimidazole (0.77 g, 4.75 mmol). The solution was stirred at 50° C. for 2 h, then 4-aminomethyl-piperidine-1-carboxylic acid tert-butyl ester (0.94 g, 4.39 mmol) was added, followed by 1,4-diazabicyclo[2,2,2]octane (1.46 g, 13 mmol). The solution was stirred at 50° C. for 16 h, allowed to cool and diluted with water (20 mL) and ethyl acetate (60 mL). The aqueous layer was removed, the organic layer washed with water (20 mL), dried over sodium sulfate and concentrated in vacuo to afford the title intermediate (1.32 g, 3.18 mmol, 73%) which was used without further purification. (m/z): [M+H]+ calcd for C23H34N4O3 415.27; found 415.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143279B2
Source datasetuspto-grants-2012_03
ORD IDord-d810b210c37d47c98e3b363d38aa15b8
Source noteuspto-grants-2012_03