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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295448Generated: October 26, 2026

Dimethylformamide → 2-Aminoquinoline-6-carbaldehyde

https://huagongshe.com/reaction/1295448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantCID 76231HCID 76231—
ReactantDiphenylpropyl phosphineHCID 53436545—
ReactantHCID 58907866HCID 58907866—
Catalystpalladium(II) acetateHCID 167845—
Product2-Aminoquinoline-6-carbaldehydeHCID 2201890624%

Reaction Steps

A mixture of 6-iodo-quinolin-2-ylamine (200 mg, 0.74 mmol), triethylamine (0.26 mL, 1.85 mmol), diphenylpropylphosphine (dpp, 17 uL, 0.074 mmol) and palladium(II) acetate (17 mg, 0.074 mmol) in dry N,N-dimethylformamide (4 mL) in pressure tube was stirred under carbon monoxide at 75 psi at room temperature for 10 min. After addition of trihexylsilane (0.53 mL, 1.5 mmol), the mixture was then stirred under carbon monoxide at 75 psi at 80° C. for 4 h. The reaction was allowed to cool to 25[ ]C and then extracted with methylene chloride (2×50 mL). The combined organic layers were successively washed with water (3×50 mL), dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 70–230 mesh, ethyl acetate) afforded 2-amino-quinoline-6-carbaldehyde (30 mg, 24%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241893B2
Source datasetuspto-grants-2007_07
ORD IDord-7e0497d3457b4dd1916693b1caee48d4
Source noteuspto-grants-2007_07