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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013598Generated: October 30, 2026

({[6-(3-Fluoro-benzenesulfonyl)-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl]-carbamoyl}-methyl)-methyl-carbamic acid benzyl ester → n-[6-(3-Fluoro-benzenesulfonyl)-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl]-2-methylamino-acetamide formate salt

https://huagongshe.com/reaction/1013598

Reaction equation

Participants

RoleNameHCIDCharge
Reactant({[6-(3-Fluoro-benzenesulfonyl)-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl]-carbamoyl}-methyl)-methyl-carbamic acid benzyl esterHCID 66651708—
CatalystPalladiumHCID 23938—
SolventFormic AcidHCID 284—
SolventMethanolHCID 887—
Productn-[6-(3-Fluoro-benzenesulfonyl)-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl]-2-methylamino-acetamide formate saltHCID 66651472144.2%

Reaction Steps

To a stirring solution of ({[6-(3-Fluoro-benzenesulfonyl)-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl]-carbamoyl}-methyl)-methyl-carbamic acid benzyl ester (0.15 g) in 20 ml methanol and 2 ml formic acid at room temperature was added 0.1 gms of 10% palladium on carbon. After stirring for three hours the mixture was filtered thru Celite and the clear filtrate was concentrated to dryness. The residue was recrystallized from ethyl acetate and diethyl ether to give 0.090 gms of N-[6-(3-Fluoro-benzenesulfonyl)-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl]-2-methylamino-acetamide formate salt: M+H=391.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981923B2
Source datasetuspto-grants-2011_07
ORD IDord-555eea2a251c4db8aa2a19210db2db52
Source noteuspto-grants-2011_07