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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402658Generated: November 3, 2026

Chloroacetyl chloride → HCID 178498778, compound

https://huagongshe.com/reaction/402658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantDimethyl malonateHCID 7943—
Reactant2-FluorobenzylamineHCID 66649—
ReactantL-ProlineHCID 145742—
Reactant1H-Pyrrolo[2,3-b]pyridine-3-carbaldehydeHCID 5372812—
ReactantHCID 86708348HCID 86708348—
SolventEthanolHCID 702—
ProductHCID 178498778HCID 17849877824%

Reaction Steps

To a solution of methyl 2-[(2-fluorobenzyl)amino]-4-oxo-4,5-dihydrofuran-3-carboxylate (0.35 g, 1.5 mmol) which similarly prepared according to the procedure described in the Example 4, First step using dimethyl malonate, chloroacetyl chloride and 2-fluorobenzylamine, and 7-azaindole-3-carboxaldehyde (0.22 g, 1.5 mmol) in ethanol (10 mL), L-proline (0.018 g, 0.15 mmol) was added at ambient temperature. The mixture was refluxed for 3 days. Cooled to ambient temperature, the precipitate was collected by filtration, washed with methanol then dried to afford the titled compound as solid (0.13 g, y. 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742113B2
Source datasetuspto-grants-2014_06
ORD IDord-46aee1c0d1d74cd1b92ba9d281cc7900
Source noteuspto-grants-2014_06