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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065820Generated: November 1, 2026

Sodium Hydroxide → 9-Amino-7-methylidenebicyclo[3.3.1]nonan-3-one

https://huagongshe.com/reaction/2065820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant(5,7-Dibromo-adamantan-2-yl)-carbamic acid tert-butyl esterHCID 16100375—
Solvent1,4-DioxaneHCID 31275—
Product9-Amino-7-methylidenebicyclo[3.3.1]nonan-3-oneHCID 67212772163.7%

Reaction Steps

(First step: Rohde, J. J. et al. Discovery and Metabolic Stabilization of Potent and Selective 2-Amino-N-(adamant-2-yl) Acetamide 11β-Hydroxysteroid Dehydrogenase Type 1 Inhibitors. J. Med. Chem. 2007, 50, 149-64). A solution of 25 (125 mg, 0.305 mmol) in dioxane (0.80 mL) was treated with 2N NaOH (0.70 mL, 1.37 mmol) and irradiated under microwaves (μw, Biotage) for 15 min at 180° C. The dioxane was removed in vacuo. The residue was dissolved in DCM, washed with water, dried (Na2SO4), filtered and concentrated in vacuo to afford 82.5 mg of crude 9-amino-7-methylene-bicyclo[3.3.1]nonan-3-one as a yellow oil, that was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288551B2
Source datasetuspto-grants-2012_10
ORD IDord-2ed546387f064a399dbfd6007682b4a8
Source noteuspto-grants-2012_10