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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828717Generated: November 2, 2026

Diisopropylethylamine → HCID 22057962, compound

https://huagongshe.com/reaction/1828717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Quinolinecarboxylic acidHCID 82571—
ReactantHCID 22057981HCID 22057981—
SolventDimethylformamideHCID 6228—
ProductHCID 22057962HCID 2205796224.4%

Reaction Steps

6-Quinolinecarboxylic acid (0.173 g) was added to a stirred suspension of N-(3-amino-4-methylphenyl)-3-dimethylaminobenzamide (0.135 g), diisopropylethylamine (0.325 ml), 2-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate(V) (0.39 g) in DMF (10 ml) and the resultant mixture was stirred at ambient temperature for 16 hours. The solvent was evaporated and the residue was dissolved in methylene chloride and washed with a saturated aqueous sodium bicarbonate solution, dried over magnesium sulphate and evaporated. The residue was triturated under a mixture of ethyl acetate and isohexane. There was thus obtained the title compound as a solid (0.052 g); NMR Spectrum: (DMSOd6) 2.24 (s, 3H), 2.95 (s, 6H), 6.89 (d, 1H), 7.25 (m, 4H), 7.6 (m, 2H), 7.85 (s, 1H), 8.12 (d, 1H), 8.4 (d, 1H), 8.52 (d, 1H), 8.65 (m, 1H), 8.99 (d, 1H), 10.11 (s, 1H), 10.16 (s, 1H); Mass Spectrum: M+H+ 425.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060700B2
Source datasetuspto-grants-2006_06
ORD IDord-8570a530be634c11b3c62c4eb5098417
Source noteuspto-grants-2006_06