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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379552Generated: October 30, 2026

Methanol → HCID 54305973, compound

https://huagongshe.com/reaction/1379552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBenzophenone imineHCID 136809—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 54238570HCID 54238570—
CatalystAcetic AcidHCID 176—
CatalystHydrochloric AcidHCID 313—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 54305973HCID 5430597383%

Reaction Steps

To a solution of (+)-(4aR)-(10bR)-4-methyl-8-(3-aminophenyl)-10b-methyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one (22 mg, 0.07 mmol), in 0.25 mL of dichloromethane was added benzophenone imine (1 eq), followed by 1 drop of 1N hydrochloric acid. The mixture was stirred at room temperature for 1 h, concentrated, and 0.5 mL of methanol and sodium cyanoborohydride (0.14 mmol) followed by two drops of glacial acetic acid was added, and the mixture was stirred for 16 h, diluted with ethyl acetate, rinsed with saturated sodium bicarbonate solution, and brine. The organic layer was dried over sodium sulfate, concentrated and chromatographed on silica gel (ethyl acetate eluent) to give, after trituration of the resulting oil from ether/hexanes, 28 mg (83%) of the title compound as a white solid. mp 109°-111°. FDMS: m/e=486. α[D]589 =+46.90 (c=0.49, methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670514
Source datasetuspto-grants-1997_09
ORD IDord-c2bc49d4c8f249e28056fb4628ce3df3
Source noteuspto-grants-1997_09