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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361685Generated: October 30, 2026

Methylamine → 11beta-Fluoro-3-hydroxy-7alpha-[5-(methylamino)-pentyl]-estra-1,3,5(10)-trien-17-one

https://huagongshe.com/reaction/361685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantHCID 15870673HCID 15870673—
SolventTetrahydrofuranHCID 8028—
Product11beta-Fluoro-3-hydroxy-7alpha-[5-(methylamino)-pentyl]-estra-1,3,5(10)-trien-17-oneHCID 15870665123.2%

Reaction Steps

5.1 g of methylamine is condensed in a solution of 6.8 g of 11β-fluoro-3-hydroxy-7α-(5-iodopentyl)-estra-1,3,5(10)-trien-17-one in 35 ml of anhydrous tetrahydrofuran at -78° C., and it is stirred overnight at room temperature in a pressurized reactor. After the pressurized reactor was opened at -20° C., it was allowed to reach room temperature to be able to evaporate excess methylamine. Then, the reaction solution is added to saturated sodium bicarbonate solution, extracted 3 times with ethyl acetate, dried on magnesium sulfate and concentrated by evaporation in a vacuum. 6.7 g of 11β-fluoro-3-hydroxy-7α-[5-(methylamino)-pentyl]-estra-1,3,5(10)-trien-17-one is obtained as crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866560
Source datasetuspto-grants-1999_02
ORD IDord-ee3c2925bc4c4a169ca6a21a99c8a622
Source noteuspto-grants-1999_02