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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341086Generated: October 30, 2026

Triethylamine → HCID 68153929, compound

https://huagongshe.com/reaction/341086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl IsocyanateHCID 12228—
ReactantHCID 68153831HCID 68153831—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68153929HCID 68153929—

Reaction Steps

2-(2-Fluorophenyl)-5-(piperidin-4-ylmethyl)-2,5-dihydro-3H-pyrazolo[4,3-c]quinolin-3-one (30 mg, 0.080 mmol) was dissolved in dichloromethane (2 ml) and tetrahydrofuran (1 ml), treated with triethylamine (0.011 ml, 0.080 mmol, 1 equiv) and methylimino(oxo)methane (4.55 mg, 0.080 mmol) were added. After 10 minutes, the mixture was concentrated in vacuo and the residue was purified by silica gel gradient chromatography (80:20 to 70:30; dichlormethane:methanol), providing the titled compound: 1H-NMR (400 MHz, d6-DMSO) δ 8.85 (1H, s), 8.21 (1H, dd, J=, 7.9, 1.6 Hz), 7.98 (1H, d, J=8.7 Hz), 7.61-7.56 (2H, m), 7.47-7.30 (4H, m), 6.37 (1H, q, J=4.2 Hz), 5.70 (2H, br s), 4.35 (2H, d, J=6.8 Hz), 3.94 (2H, br d, J=13.6 Hz), 2.52 (3H, d, J=4.9 Hz), 2.13-2.02 (1H, m), 1.49 (2H, br d, J=12.3 Hz), 1.25-1.13 (2H, m) ppm; high resolution mass spectrometry (ES+) m/z 434.1998 [(M+H)+; calculated for C24H25FN5O2: 434.1987].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895580B2
Source datasetuspto-grants-2014_11
ORD IDord-09f6af536390420f91c460a8add45ac6
Source noteuspto-grants-2014_11