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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802472Generated: November 1, 2026

Triethylamine → HCID 59436093, compound

https://huagongshe.com/reaction/1802472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonyl chlorideHCID 79000—
ReactantHCID 59436027HCID 59436027—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59436093HCID 59436093—

Reaction Steps

To a solution of 5-{[5-(aminomethyl)-2-methylphenyl]amino}-9-fluorobenzo[c]-2,6-naphthyridin-1(2H)-one (35 mg, 0.10 mmol) in THF (1.0 mL) at 0° C. was added triethylamine (0.03 mL, 0.20 mmol) and trifluoromethanesufonyl chloride (0.01 mL, 0.11 mmol). The reaction was stirred for one hour and then quenched by the addition of citric acid. The mixture was extracted with EtOAc/water and the extracts were washed with brine, dried over MgSO4 and concentrated in vacuo. Purification by silica gel column chromatographpy (0-10% MeOH/CH2Cl2) afforded the title compound. 1H NMR (600 MHz, CD6SO) δ 12.21 (d, 1H), 9.92 (s, 1H), 9.45 (dd, 1H), 8.85 (s, 1H), 7.68 (m, 1H), 7.45 (m, 1H), 7.34-7.38 (m, 2H), 7.26 (d, 1H), 7.22 (d, 1H), 7.09 (d, 1H), 4.32 (s, 2H), 2.12 (s, 3H). LRMS (ESI) calc'd for C21H16F4N4O3 [M+H]+, 481.1; found 481.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349865B2
Source datasetuspto-grants-2013_01
ORD IDord-2cc83fa9b9c14b0ea548276989bf71ce
Source noteuspto-grants-2013_01