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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675945Generated: October 31, 2026

Diisopropylethylamine → HCID 25226444, compound

https://huagongshe.com/reaction/1675945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPropylphosphonic acidHCID 204484—
Reactant1-(1-Methyl-1,2,3,4-tetrahydroquinolin-6-yl)methanamineHCID 1112172—
ReactantHCID 58539042HCID 58539042—
SolventAcetonitrileHCID 6342—
ProductHCID 25226444HCID 25226444—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 5′-methyl-6-(3-methyl-1H-pyrazol-1-yl)-3,3′-bipyridine-5-carboxylic acid (5-2, 0.025 g, 0.085 mmol) and 1-(1-methyl-1,2,3,4-tetrahydroquinolin-6-yl)methanamine (0.015 g, 0.085 mmol) in ACN (0.85 mL) was added 1-propylphosphonic acid cyclic anhydride (T3P, 0.15 mL, 0.255 mmol) followed by Hunig's base (0.089 mL, 0.51 mmol) and the system was stirred at 40° C. for 1 h in an oil bath. The reaction mixture was cooled and partitioned between EtOAc and water, washed with saturated sodium bicarbonate and dried over magnesium sulfate. The reaction mixture was filtered, concentrated and purified via normal phase chromatography (0→10% MeOH in EtOAc) to afford the title compound (5-3) as a bone powder. 1H NMR (500 MHz, CDCl3) δ 8.68 (m, 1H), 8.51 (m, 1H), 8.29 (m, 1H), 8.22 (m, 1H), 7.72 (m, 1H), 7.12 (m, 1H), 7.0 (m, 1H), 6.90 (m, 1H), 6.54 (m, 1H), 6.27 (m, 1H), 4.46 (m, 2H), 3.22(m, 2H), 2.88 (s, 3H), 2.74 (m, 2H), 2.44 (s, 3H), 2.28 (s, 3H), 1.97 (m, 2H). HRMS [M+H] C27H28N6O calc'd 453.2391, found 453.2397.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003797B2
Source datasetuspto-grants-2011_08
ORD IDord-6d08999fe95d4d08b890d76d14e8e4d4
Source noteuspto-grants-2011_08