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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502936Generated: October 26, 2026

(1S*,2R*,4R*)-[4-Azido-2-(4-methylsulfanyl-benzenesulfonylmethyl)-cyclohexyl]-carbamic acid tert-butyl ester → (1S*,2R*,4R*)-[4-amino-2-(4-methylsulfanyl-benzenesulfonylmethyl)-cyclohexyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/502936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1S*,2R*,4R*)-[4-Azido-2-(4-methylsulfanyl-benzenesulfonylmethyl)-cyclohexyl]-carbamic acid tert-butyl esterHCID 86590249—
ReactantHCID 178418361HCID 178418361—
CatalystPd barium sulfateHCID 16218511—
SolventMethanolHCID 887—
Product(1S*,2R*,4R*)-[4-amino-2-(4-methylsulfanyl-benzenesulfonylmethyl)-cyclohexyl]-carbamic acid tert-butyl esterHCID 6846836699.9%

Reaction Steps

±(1S*,2R*,4R*)-[4-Azido-2-(4-methylsulfanyl-benzenesulfonylmethyl)-cyclohexyl]-carbamic acid tert-butyl ester (from example 55d), (100 mg) was dissolved in MeOH (1 ml) prior to the addition of 5% Pd/BaSO4 (120 mg). A hydrogen balloon was added and the solution was stirred for 1.5 h. The palladium was filtered off and the solution was concentrated to give ±(1S*,2R*,4R*)-[4-amino-2-(4-methylsulfanyl-benzenesulfonylmethyl)-cyclohexyl]-carbamic acid tert-butyl ester (94 mg). MS found: (M+H)+=415.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776884B2
Source datasetuspto-grants-2010_08
ORD IDord-1ea1063128f04997b28bf099f8aea323
Source noteuspto-grants-2010_08