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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446719Generated: October 30, 2026

Dimethylformamide → HCID 58293835, compound

https://huagongshe.com/reaction/446719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 67027086HCID 67027086—
SolventDichloromethaneHCID 6344—
ProductHCID 58293835HCID 5829383531.8%

Reaction Steps

To a solution of Compound 1036 (2.25 g, 7.885 mmol) in DCM (35 mL) was added 0.1 mL of DMF followed by addition of oxalyl chloride (1.502 g, 1.032 mL, 11.83 mmol). The reaction mixture was stirred at RT for 1 hour and the volatiles were removed in vacuo. The residue was taken up in benzene and the volatiles were again removed in vacuo (2×), followed by drying under vacuum. The residue was taken up in dry DCM (35 mL) and AlCl3 (3.679 g, 27.59 mmol) was added at RT. The mixture was stirred at RT for 1.5 hours and the reaction quenched with ethanol. The resulting solution was poured into ice water and extracted with DCM (2×). The combined organic layers were dried over Na2SO4, concentrated under vacuum, and the residue purified by silica gel chromatography, using a 5%-20% ethyl acetate/hexanes gradient as eluant, to produce ethyl 7-ethyl-4-oxo-7,8-dihydro-4H-thieno[2,3-d]azepine-6(5H)-carboxylate (Compound 1037, 671 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481524B2
Source datasetuspto-grants-2013_07
ORD IDord-aae349ccdeca46cab16358327161d829
Source noteuspto-grants-2013_07