Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610650Generated: November 1, 2026

Sodium hydride → HCID 19601673, compound

https://huagongshe.com/reaction/610650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantPropane, 1-bromo-3-fluoro-HCID 67699—
ReactantHCID 19601666HCID 19601666—
SolventDimethylformamideHCID 6228—
ProductHCID 19601673HCID 1960167337%

Reaction Steps

To a solution of 1-(3-iodophenyl)-N-methyl-3-isoquinolinecarboxamide (22 mg, 0.06 mmol) in DMF (4.6 mL) was added 60% NaH (16 mg, 0.39 mmol) in one portion. The mixture was stirred under Ar at room temperature for 15 min. Then, 3-fluoropropyl bromide (29 μl, 0.39 mmol) was added. After stirring at room temperature for 20 h, 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 (4.4 mg, 37%). 1H NMR (CDCl3) d 2.04-2.24 (m, 2 H, CH2), 3.16, 3.18 (two s, total 3 H, N-methyl), 3.60-3.75 (m, 2 H, N--CH2), 4.25-4.70 (qt, J=67.8, 47.1, 5.7 Hz, 2 H, CH2F), 7.20-7.30 (m, 1 H, aromatic), 7.55-7.65 (m, 2 H, aromatic), 7.73 (t, J=7.2 Hz, 1 H, aromatic), 7.83 (d, J=7.8 Hz, 1 H, aromatic), 7.94 (d, J=8.4 Hz, 1 H, aromatic), 7.98-8.09 (m, 2 H, aromatic), 8.12 (s, 1 H, aromatic). HRMS calcd. for C20H18FIN2O: 448.0448. Found: 448.0461

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998624
Source datasetuspto-grants-1999_12
ORD IDord-ba59c4aeddeb4d8a8e900ec818b2c5ef
Source noteuspto-grants-1999_12