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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339023Generated: October 30, 2026

Hydrochloric Acid → N-isopropyl-2,8-dimethylquinoline-7-carboxamide

https://huagongshe.com/reaction/339023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsopropylamineHCID 6363—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant2,8-Dimethylquinoline-7-carboxylic acidHCID 70983571—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductN-isopropyl-2,8-dimethylquinoline-7-carboxamideHCID 7098393193%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 2,8-dimethylquinoline-7-carboxylic acid (0.20 g, 0.994 mmol), isopropylamine (0.102 mL, 1.19 mmol) and HATU (0.491 g, 1.29 mmol) in anhydrous MeCN (5 mL) under a nitrogen atmosphere was cooled to 0° C. in an ice bath. To the cooled mixture was added dropwise DIEA (0.69 mL, 3.98 mmol) and the resulting mixture stirred at ambient temperature for 18 hours. The mixture was diluted with water, neutralized with aqueous 1N HCl and extracted with ethyl acetate. The combined organic extracts were washed with water and brine, dried (MgSO4), filtered and concentrated under reduced pressure. The residue was purified by reverse phase chromatography (Biotage SP4, 25M C-18, 5-60% MeCN—H2O) to afford N-isopropyl-2,8-dimethylquinoline-7-carboxamide (0.223 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889704B2
Source datasetuspto-grants-2014_11
ORD IDord-b518f8e5a55c45519ab8cf368d964e54
Source noteuspto-grants-2014_11