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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72142Generated: October 28, 2026

tert-butyl (1R,5S)-3-oxo-8-azabicyclo[3.2.1]octane-8-carboxylate → tert-Butyl 3-amino-8-azabicyclo[3.2.1]octane-8-carboxylate

https://huagongshe.com/reaction/72142

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (1R,5S)-3-oxo-8-azabicyclo[3.2.1]octane-8-carboxylateHCID 688612—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
Producttert-Butyl 3-amino-8-azabicyclo[3.2.1]octane-8-carboxylateHCID 2257051998.9%

Reaction Steps

A stirred mixture of Boc-nortropinone (287 mg, 1.3 mmol), NH4OAc (1.96 g, 25.5 mmol), NaCNBH3 (800 mg, 12.7 mmol) and MeOH (20 mL) was heated at reflux for 2 h. The mixture was concentrated, the residue was diluted with 0.5 M aq NaOH (30 mL) and extracted with CH2Cl2 (2×50 mL). The combined organic phase was washed with brine (20 mL), dried over Na2SO4 and concentrated to afford tert-butyl 3-amino-8-azabicyclo[3.2.1]octane-8-carboxylate (291 mg, quant) as a mixture of isomers. LC-MS Method 1 tR=0.88 min, m/z=227.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828985B2
Source datasetuspto-grants-2014_09
ORD IDord-e04684fd343049fd920a9a14980402b7
Source noteuspto-grants-2014_09