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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446009Generated: October 27, 2026

Triethylamine → 4-[(11-Acetoxy-6,17-dihydroxy-1-methoxymethyl-10,13-dimethyl-3,7-dioxo-1,7,10,11,12,13,14,15,16,17-decahydro-2-oxa-cyclopenta[a]phenanthren-4-ylidenemethyl)-methyl-amino]-butyric acid

https://huagongshe.com/reaction/1446009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant17beta-Hydroxy wortmanninHCID 9867340—
Reactant4-(Methylamino)butyric acid hydrochlorideHCID 12626654—
SolventDichloromethaneHCID 6344—
Product4-[(11-Acetoxy-6,17-dihydroxy-1-methoxymethyl-10,13-dimethyl-3,7-dioxo-1,7,10,11,12,13,14,15,16,17-decahydro-2-oxa-cyclopenta[a]phenanthren-4-ylidenemethyl)-methyl-amino]-butyric acidHCID 68542425—

Reaction Steps

To a solution of 100 mg (0.23 mmol) 17-hydroxywortmannin and triethylamine (65 μL, 0.46 mmol) in 2 mL CH2Cl2 is added 4-(methylamino)butyric acid hydrochloride (71 mg, 0.46 mmol). The reaction mixture is stirred at room temperature for 12 hours and then concentrated in vacuo. The residue is dissolved in EtOAc and precipitated with hexane. The precipitate is washed two times with hexane to give the product as a yellow solid. MS (ESI) m/z 549 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666901B2
Source datasetuspto-grants-2010_02
ORD IDord-ff486d22e1334ef188df2578b602e15e
Source noteuspto-grants-2010_02