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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445979Generated: October 25, 2026

2-(tert-Butylamino)ethanol → (1E,4S,4aR,5R,6aS,7S)-1-{[tert-butyl(2-hydroxyethyl)amino]methylene}-7,11-dihydroxy-4-(methoxymethyl)-4a,6a-dimethyl-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/1445979

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(tert-Butylamino)ethanolHCID 78361—
Reactant17beta-Hydroxy wortmanninHCID 9867340—
SolventDichloromethaneHCID 6344—
Product(1E,4S,4aR,5R,6aS,7S)-1-{[tert-butyl(2-hydroxyethyl)amino]methylene}-7,11-dihydroxy-4-(methoxymethyl)-4a,6a-dimethyl-2,10-dioxo-1,2,4,4a,5,6,6a,7,8,9,9a,10-dodecahydroindeno[4,5-h]isochromen-5-yl acetateHCID 1151960648.7%

Reaction Steps

To a solution of 50 mg (0.12 mmol) 17-hydroxywortmannin in 0.5 mL CH2Cl2 is added 28.1 mg (0.24 mmol) 2-(tert-butylamino)-ethanol. The reaction mixture is stirred at room temperature overnight. CH2Cl2 is removed in vacuo. The residue is triturated with diethyl ether (Et2O) to give 32 mg (48.7%) product as an orange powder. MS (ESI) m/z 548.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666901B2
Source datasetuspto-grants-2010_02
ORD IDord-c7ffb7f56b914ec7a230738caf7e665d
Source noteuspto-grants-2010_02