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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627379Generated: October 31, 2026

HCID 67356417, compound → 9-Boc-3,9-diaza-bicyclo[3.3.1]nonane

https://huagongshe.com/reaction/627379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67356417HCID 67356417—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Product9-Boc-3,9-diaza-bicyclo[3.3.1]nonaneHCID 5459553949.7%

Reaction Steps

A mixture of benzyl-3,9-diaza-bicyclo[3.3.1]nonane-9-carboxylic acid tert-butyl ester (477 mg, 1.51 mmol, 1.0 eq) and palladium hydroxide on carbon (466 mg) in ethanol (10 mL) was stirred with hydrogenation under balloon pressure until no more hydrogen uptake. The reaction was then filtered through celite and concentrated under reduced pressure. The crude was purified using chromatography (MeOH/Ethyl Acetate) which gave 3,9-Diaza-bicyclo[3.3.1]nonane-9-carboxylic acid tert-butyl ester (170 mg) in 47% yield. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.49 (s, 11H) 1.57-1.70 (m, 1H) 1.70-1.79 (m, 2H) 1.79-2.01 (m, 2H) 2.43-2.58 (m, J=19.14, 12.69, 6.32, 6.32 Hz, 1H) 2.93-3.05 (m, 2H) 3.05-3.18 (m, 2H) 3.99 (br. s., 1H) 4.11 (br. s., 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309252B2
Source datasetuspto-grants-2016_04
ORD IDord-7d526196e8b04e669af1d13ab65b6f17
Source noteuspto-grants-2016_04