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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490273Generated: November 2, 2026

Dimethylformamide → HCID 14366447, compound

https://huagongshe.com/reaction/1490273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 178524012HCID 178524012—
ProductHCID 14366447HCID 1436644739.3%

Reaction Steps

A mixture of quindoline-11-carboxylic acid (2.6 g, 10 mmol) from Example 1, DMF (25 mL), KOH (2.24 g, 40 mmol), BaO (6.27 g, 40 mmol) and methyl iodide (9.7 mL, 130 mmol) was stirred at room temperature for 48 hours, then partitioned between benzene (60 mL) and water (100 mL). The benzene layer was washed with water (2×60 mL), dried and concentrated. The residue was recrystallized from hexane to afford 1.14 g (39.3%) of the title compound as light yellow crystals, mp 127° C.; 1H NMR (CDCl3) δ 8.49 (d, J=8.0, 1H), 8.31(d, J=8.0, 1H), 7.95 (d, J=8.4, 1H), 7.68-7.55 (m, 3H), 7.42 (d,J=8.0, 1H), 7.37 (t, J=7.2, 1H), 4.14 (s, 3H), 3.79 (s, 3H); 13C NMR (CDCl3) δ 167.98, 146.93, 145.64, 143.25, 130.27, 129.66, 126.52, 123.55, 122.92, 122.02, 121.28, 120.42, 115.77, 108.70, 52.71, 30.75; MS (EI, m/z) 290.1 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05681958
Source datasetuspto-grants-1997_10
ORD IDord-493968b16b304736b0d8f26a3b3a7fa2
Source noteuspto-grants-1997_10