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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009954Generated: November 2, 2026

HCID 57847118, compound → HCID 57846922, compound

https://huagongshe.com/reaction/1009954

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 diisopropyl ether gave the title compound (70 mg, 17%) as pale-brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973163B2
Source datasetuspto-grants-2011_07
ORD IDord-f8cac6e4d46d44e983dd2bc1de198761
Source noteuspto-grants-2011_07