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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465561Generated: November 2, 2026

Triethylamine → HCID 71586282, compound

https://huagongshe.com/reaction/1465561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsonicotinoyl chloride hydrochlorideHCID 12262826—
ReactantHCID 86690863HCID 86690863—
SolventDichloromethaneHCID 6344—
ProductHCID 71586282HCID 7158628252.2%

Reaction Steps

To a solution of 4-{4-((5-methoxypyridin-2-yl)oxy)-2,6-dimethylphenyl}thiazol-2-amine (18-4, 0.10 g, 0.31 mmol) in CH2Cl2 (5.0 mL) was added triethylamine (0.50 mL, 3.6 mmol) followed by isonicotinoyl chloride hydrochloride (0.15 g, 0.80 mmol). The reaction mixture was stirred at room temperature overnight. The solution was concentrated under reduced pressure and added with water. The resultant precipitate was filtered and recrystallized in toluene to give N-(4-{4-((5-methoxypyridin-2-yl)oxy)-2,6-dimethylphenyl}thiazol-2-yl)isonicotinamide (18, 0.070 g) as light yellow solids in 52% yield: 1H NMR (500 MHz, DMSO-d6) δ 8.81 (d, J=5.5 Hz, 2 H), 7.99 (dt, J=3.1, 1.5 Hz, 2 H), 7.92 (d, J=3.1 Hz, 1 H), 7.52 (dt, J=5.7, 3.2 Hz, 1 H), 7.20 (s, 1 H), 7.00 (d, J=8.8 Hz, 1 H), 6.81 (s, 2 H), 3.81 (s, 3 H), 2.08 (s, 6 H). ESI-MS: m/z 433.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999983B2
Source datasetuspto-grants-2015_04
ORD IDord-46a09750f6fa4b318ed62354d315c5b4
Source noteuspto-grants-2015_04