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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826889Generated: November 1, 2026

Dicyclohexylcarbodiimide → HCID 22136364, compound

https://huagongshe.com/reaction/1826889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant1-AdamantanolHCID 64152—
ReactantQuinoline-3-carboxylic acidHCID 80971—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 22136364HCID 22136364—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 1-adamantanol (152 mg, 1.0 mmol), 3-quinolinecarboxylic acid (173 mg, 1.0 mmol), and dimethylaminopyridine (122 mg, 1.0 mmol) in dichloromethane (2 mL) and N,N-dimethylformamide (2 mL) was cooled to 0° C. 1,3-Dicyclohexylcarbodiimide (227 mg, 1.1 mmol) in dichloromethane (1 mL) was added in one portion. The reaction mixture was stirred at 25° C. for 20 h. The reaction mixture was then diluted with dichloromethane (40 mL) and washed with 1 M sodium hydroxide (3×30 mL). The organic layer was dried (anhydrous magnesium sulfate), filtered through Celite, and rotary evaporated. The resulting material was purified by spinning thin-layer chromatography (3% methanol in chloroform). The purest fraction was rotary evaporated, and the resulting material was recrystallized from ethanol. This provided 42 mg (14%) of (101):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053104B2
Source datasetuspto-grants-2006_05
ORD IDord-8f42a0d8a0574290952b9f576510f9e2
Source noteuspto-grants-2006_05