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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879203Generated: October 30, 2026

(+/-)-tert-butyl ((1R,5S,6R)-6-methoxy-5-methyl-3-(3-nitropyridin-4-yl)cyclohex-2-en-1-yl)carbamate → HCID 86705250, compound

https://huagongshe.com/reaction/879203

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+/-)-tert-butyl ((1R,5S,6R)-6-methoxy-5-methyl-3-(3-nitropyridin-4-yl)cyclohex-2-en-1-yl)carbamateHCID 86705248—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 86705250HCID 8670525015%
ProductHCID 86705251HCID 8670525112%

Reaction Steps

To a solution of (+/−)-tert-butyl ((1R,5S,6R)-6-methoxy-5-methyl-3-(3-nitropyridin-4-yl)cyclohex-2-en-1-yl)carbamate (1.0 equiv.) in degassed EtOH (0.10 M) was added Pd/C (0.1 equiv.). The mixture was purged with H2, and allowed to to stir under an atm of H2 overnight at RT. The reaction was filtered through a pad of celite and the cake was washed with MeOH. The organics were concentrated and purified by ISCO SiO2 chromatography. Purification was completed via SFC (30% MeOH, 100 mL/min, AD column) to yield tert-butyl ((1S,2S,3R,5S)-5-(3-aminopyridin-4-yl)-2-methoxy-3-methylcyclohexyl)carbamate (15% yield, 99% ee) and tert-butyl ((1R,2R,3S,5R)-5-(3-aminopyridin-4-yl)-2-methoxy-3-methylcyclohexyl)carbamate (12% yield, 99% ee). LC/MS (m/z)=336.3 (MH+), Rt=0.58 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987457B2
Source datasetuspto-grants-2015_03
ORD IDord-497e8d1df6ae4388b52cc950ebb38378
Source noteuspto-grants-2015_03