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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445993Generated: October 27, 2026

N'-(3-(Dimethylamino)propyl)-N,N-dimethyl-1,3-propanediamine → Acetic acid 4-{[bis-(3-dimethylamino-propyl)-amino]-methylene}-6,17-dihydroxy-1-methoxymethyl-10,13-dimethyl-3,7-dioxo-1,3,4,7,10,11,12,13,14,15,16,17-dodecahydro-2-oxa-cyclopenta[a]phenanthren-11-yl ester

https://huagongshe.com/reaction/1445993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN'-(3-(Dimethylamino)propyl)-N,N-dimethyl-1,3-propanediamineHCID 81207—
Reactant17beta-Hydroxy wortmanninHCID 9867340—
SolventDichloromethaneHCID 6344—
ProductAcetic acid 4-{[bis-(3-dimethylamino-propyl)-amino]-methylene}-6,17-dihydroxy-1-methoxymethyl-10,13-dimethyl-3,7-dioxo-1,3,4,7,10,11,12,13,14,15,16,17-dodecahydro-2-oxa-cyclopenta[a]phenanthren-11-yl esterHCID 68541248—

Reaction Steps

To a solution of 100 mg (0.23 mmol) 17-hydroxywortmannin in 2 mL CH2Cl2 is added 3,3′-iminobis(N,N-dimethylpropylamine) (104 μL, 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 619 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666901B2
Source datasetuspto-grants-2010_02
ORD IDord-9aaed09c98654e8190f129a1eacb3458
Source noteuspto-grants-2010_02