Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610651Generated: November 1, 2026

Sodium hydride → HCID 19601663, compound

https://huagongshe.com/reaction/610651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantPropane, 1-bromo-3-fluoro-HCID 67699—
ReactantHCID 19601665HCID 19601665—
SolventDimethylformamideHCID 6228—
ProductHCID 19601663HCID 1960166340.9%

Reaction Steps

To a solution of 1-(4-iodophenyl)-N-methyl-3-isoquinolinecarboxamide (25 mg, 0.06 mmol) in DMF (4 mL) was added 60% NaH (10 mg, 0.25 mmol) in one portion. The mixture was stirred under Ar at room temperature for 30 min. Then, 3-fluoropropyl bromide (20 μl, 0.27 mmol) was added. After stirring at room temperature for overnight, the mixture was quenched by adding H2O (5 mL). The mixture was extracted with CH2Cl2 (3×15 mL). The combined organic layers were dried (MgSO4), filtered. The filtrate was concentrated in vacuo. The residue was chromatographed (SiO2, 30% ethyl acetate/hexane, 0.035% Et3N), thereby affording a semisolid (11 mg, 40%). 1H NMR (CDCl3) d 2.01-2.22 (m, 2 H, CH2), 3.15, 3.17 (two s, total 3 H, N-methyl), 3.60-3.76 (m, 2 H, N--CH2), 4.22-4.76 (qt, J=77.7, 47.1, 5.7 Hz, 2 H, CH2F), 7.36-7.47 (m, 1 H, aromatic), 7.50-7.81 (m, 4 H, aromatic), 7.82-7.99 (m, 2 H, aromatic), 7.83-8.16 (m, 2 H, aromatic). HRMS calcd. for C20H18FIN2O: 448.0448. Found: 448.0435.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998624
Source datasetuspto-grants-1999_12
ORD IDord-1d1a693db1184be5a7bf586e6b9943e8
Source noteuspto-grants-1999_12