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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550291Generated: October 28, 2026

Diethyl Pyrocarbonate → HCID 57846915, compound

https://huagongshe.com/reaction/550291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl PyrocarbonateHCID 3051—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant(+)-cis-2-Benzamidocyclohexanecarboxylic AcidHCID 1268229—
ReactantHCID 57846973HCID 57846973—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57846915HCID 5784691562%

Reaction Steps

To a mixture of (3aR*,4S*,9bS*)-4-phenyl-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinoline (620 mg, 2.47 mmol), (1S,2R)-2-(benzoylamino)cyclohexanecarboxylic acid (671 mg, 2.7% mmol), triethylamine (0.72 ml, 5.2 mmol), acetonitrile (17 ml) and tetrahydrofuran (17 ml) was added dropwise DEPC (440 mg, 2.7 mmol) under ice-cooling, and the mixture was stirred for 10 min. The mixture was allowed to return to room temperature and the mixture was stirred for 1 hr. Saturated aqueous sodium hydrogen carbonate solution was added to the reaction mixture and the mixture was extracted with ethyl acetate. The extract was dried (over anhydrous Na2SO4), and the solvent was evaporated. The residue was subjected to column chromatography using silica gel (30 g), and eluted with hexane-ethyl acetate (9:1-7:3, v/v) to give the title compound (735 mg, 62%) as an amorphous form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943770B2
Source datasetuspto-grants-2011_05
ORD IDord-fd0af972c3af47df83151065d98d5032
Source noteuspto-grants-2011_05