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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495140Generated: October 29, 2026

Trifluoroacetic acid → HCID 86596927, compound

https://huagongshe.com/reaction/495140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 9795003HCID 9795003—
ReactantIsonicotinoyl chloride hydrochlorideHCID 12262826—
SolventDichloromethaneHCID 6344—
ProductHCID 86596927HCID 8659692730%

Reaction Steps

The trifluoroacetic acid salt of 4-(3-amino-propoxy)-6-chloro-1-benzopyran-2-one (0.272 mmol, 0.10 g) is dissolved in 3 mL of DCM and is added enough DIEA to bring the pH to ˜9 as measured by wet pH paper. Isonicotinoyl chloride hydrochloride is added (0.50 mmol, 0.089 g) and the reaction is stirred at ambient temperature overnight. The reaction mixture is evaporated under reduced pressure and the crude material is purified by HPLC to obtain the title compound as the trifluoroacetic acid salt (39 mg, 30%). 1H NMR (DMSO-d6, 300 MHz) δ 8.93 (1H, br t), 8.73 (2H, br d), 7.80 (2H, m), 7.76 (1H, d, J=2.5 Hz), 7.69 (1H, dd, J=2.5, 8.75 Hz), 7.45 (1H, d, J=8.75 Hz), 5.97 (1H, s), 4.31 (2H, t, J=5.75 Hz), 3.51 (2H, q, J=6.5 Hz), 2.11 (2H, m); MS (ESI, Pos.) calcd for C18H15ClN2O4 m/z [M+H]=359.1, found 359.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538233B2
Source datasetuspto-grants-2009_05
ORD IDord-c75b64270a8648b5b0bfaa14a4b1cc4f
Source noteuspto-grants-2009_05