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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550313Generated: October 29, 2026

HCID 57847118, compound → HCID 57846922, compound

https://huagongshe.com/reaction/550313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57847118HCID 57847118—
ReactantHCID 68576547HCID 68576547—
CatalystHCID 178418406HCID 178418406—
SolventTolueneHCID 1140—
ProductHCID 57846922HCID 5784692217%

Reaction Steps

A mixture of N-((1R,2S)-2-{[(3aR*,4R*,9bR*)-4-(3-thienyl)-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinolin-1-yl]carbonyl}cyclohexyl)benzamide and N-((1R,2S)-2-{[(3aS*,4R*,9bS*)-4-(3-thienyl)-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinolin-1-yl]carbonyl}cyclohexyl)benzamide (422 mg, 0.87 mmol) was dissolved in toluene (30 ml), manganese dioxide (7.6 g, 87 mmol) was added and the mixture was refluxed overnight. The reaction mixture was filtered through celite and washed with methanol. The filtrate was concentrated under reduced pressure. The residue was subjected to column chromatography using silica gel (30 g), and eluted with hexane-ethyl acetate (9:1-2:1, v/v). Crystallization from diisopropy ether gave the title compound (70 mg, 17%) as pale-brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943770B2
Source datasetuspto-grants-2011_05
ORD IDord-f7ea283eec4c4c9abcdd6b385ef3f028
Source noteuspto-grants-2011_05