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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373098Generated: October 31, 2026

[(1S,2S,4R)-1-Benzyl-4-(bicyclo[2.2.1]hept-2-ylcarbamoyl)-2-hydroxy-7-methyl-oct-6-enyl]carbamic acid tert-butyl ester → [(1S,2S,4R)-1-Benzyl-4-(bicyclo[2.2.1]hept-2-ylcarbamoyl)-2-hydroxy-7-methyl-octyl]carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1373098

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[(1S,2S,4R)-1-Benzyl-4-(bicyclo[2.2.1]hept-2-ylcarbamoyl)-2-hydroxy-7-methyl-oct-6-enyl]carbamic acid tert-butyl esterHCID 69507684—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product[(1S,2S,4R)-1-Benzyl-4-(bicyclo[2.2.1]hept-2-ylcarbamoyl)-2-hydroxy-7-methyl-octyl]carbamic acid tert-butyl esterHCID 6950837593%

Reaction Steps

[(1S,2S,4R)-1-Benzyl-4-(bicyclo[2.2.1]hept-2-ylcarbamoyl)-2-hydroxy-7-methyl-oct-6-enyl]-carbamic acid tert-butyl ester (D6) (1.61 g, 3.33 mmol) in methanol (30 ml) was hydrogenated over 10% Pd/C (300 mg) for 3.75 h. The catalyst was filtered and the filtrate evaporated to afford D7 (93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160905B2
Source datasetuspto-grants-2007_01
ORD IDord-013efa6b7b37405996e5fce39f55b4b6
Source noteuspto-grants-2007_01