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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377626Generated: October 26, 2026

Indole → HCID 18656668, compound

https://huagongshe.com/reaction/1377626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantPhenylseleninyl benzeneseleninateHCID 87253—
ReactantHCID 56979168HCID 56979168—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18656668HCID 1865666853.2%

Reaction Steps

A solution of 1.0 g (2.99 mmol) of (2aR,4S)-6-(3-pyridyl)-4-(di-n-propylamino)-1,2,2a,3,4,5-hexahydrobenz[cd]indole and 1.0 g (9 mmol) of indole in 50 ml of THF was treated at 0° C. with 0.61 g (1.70 mmol) of benzeneseleninic anhydride. The resulting solution was allowed to warm to room temperature. After 2 hours the reaction solution was diluted with water and the product was extracted into methylene chloride. The methylene chloride was evaporated and the resulting residue was taken up in aqueous tartaric acid. This acidic solution was washed with methylene chloride, then basified with 5M sodium hydroxide solution. The product was extracted into methylene chloride. After evaporating the methylene chloride the product was chromatographed over 25 g of silica gel using 10% ethyl acetate in toluene followed by 1:1 ethyl acetate/toluene as eluent. The material from the column was crystallized from toluene/hexane to afford 0.53 g of title compound. m.p. 185°-186° C. MS (FD) 334 [α]D -52.0° (MeOH)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665743
Source datasetuspto-grants-1997_09
ORD IDord-768c60cab0f7408ea8e374d788d78bfd
Source noteuspto-grants-1997_09