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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379481Generated: October 29, 2026

Dicyclohexylcarbodiimide → HCID 15230625, compound

https://huagongshe.com/reaction/2379481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant3,5-Di-tert-butyl-4-hydroxybenzoic acidHCID 15007—
ReactantHCID 15035245HCID 15035245—
SolventDichloromethaneHCID 6344—
ProductHCID 15230625HCID 1523062547.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3,5-di-tert-butyl-4-hydroxybenzoic acid (220 mg) in dichloromethane (20 ml) was dropwise added dicyclohexylcarbodiimide (DCC) (180 mg) under stirring at 0° C. The mixture was stirred at 0° C. for 15 minutes. Then, 3-amino-6-chloro-4-(2,3,4-trimethoxyphenyl) quinoline (250 mg) was added to this mixture. The resultant mixture was stirred at 0° C. for an hour and at room temperature for two days. After the residue was filtered off, the filtrate was diluted with water and extracted with dichloromethane. The dichloromethane layer was washed with an aqueous sodium hydroxide solution, diluted with hydrochloric acid and water in this order and dried (MgSO4). The solvent was removed and the residue was purified by a silica gel column chromatography with hexane-ethyl acetate (3:1, V/V), and then crystallized from isopropyl ether to obtain 3-(3,5-di-tert-butyl-4-hydroxybenzamido)-6-chloro-4-(2,3,-4-trimethoxyphenyl) quinoline (199 mg, 47.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05362742
Source datasetuspto-grants-1994_11
ORD IDord-8058a6a26b304701ac27615d4119c2a3
Source noteuspto-grants-1994_11