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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445981Generated: October 25, 2026

N,1-dimethylpyrrolidin-3-amine → (1e,4s,4Ar,5r,6as,7s)-7,11-dihydroxy-4-(methoxymethyl)-4a,6a-dimethyl-1-{[methyl(1-methylpyrrolidin-3-yl)amino]methylene}-2,10-dioxo-1,2,4,4a,5,6,6a,7,8,9,9a,10-dodecahydroindeno[4,5-h]isochromen-5-yl acetate

https://huagongshe.com/reaction/1445981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,1-dimethylpyrrolidin-3-amineHCID 2758520—
Reactant17beta-Hydroxy wortmanninHCID 9867340—
SolventDichloromethaneHCID 6344—
Product(1e,4s,4Ar,5r,6as,7s)-7,11-dihydroxy-4-(methoxymethyl)-4a,6a-dimethyl-1-{[methyl(1-methylpyrrolidin-3-yl)amino]methylene}-2,10-dioxo-1,2,4,4a,5,6,6a,7,8,9,9a,10-dodecahydroindeno[4,5-h]isochromen-5-yl acetateHCID 1151225838.3%

Reaction Steps

To a solution of 50 mg (0.12 mmol) 17-hydroxywortmannin in 0.5 mL CH2Cl2 is added 27.4 mg (0.24 mmol) N,N′-dimethyl-3-aminopyrrolidine. The reaction mixture is stirred at room temperature overnight. CH2Cl2 is removed in vacuo. The residue is triturated with Et2O to give 25 mg (38%) product as an orange powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666901B2
Source datasetuspto-grants-2010_02
ORD IDord-e0c3e1d909184f1f902433fe0c7071c5
Source noteuspto-grants-2010_02