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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070959Generated: October 31, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → methyl 3-(azidomethyl)-5-(N-methylmethylsulfonamido)benzoate

https://huagongshe.com/reaction/2070959

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantMethyl 3-(hydroxymethyl)-5-[methyl(methylsulfonyl)amino]benzoateHCID 57815142—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Productmethyl 3-(azidomethyl)-5-(N-methylmethylsulfonamido)benzoateHCID 86647414—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirring solution of 130 mg (0.475 mmol) of methyl 3-(hydroxymethyl)-5-(N-methylmethylsulfonamido)benzoate in 7 mL of toluene and 4 mL of THF was added 120 μL of diphenyl phosphoryl azide (DPPA). The solution was cooled to 0° C. and 86 μL (0.568 mmol) of 1,8-diazabicyclo[5.4.0]-undec-7-ene (DBU) was added. The ice bath was removed, and stirring was continued with warming to room temperature. After about 16 h, the solution was diluted with EtOAc and H2O, and 1N HCl was added to a pH=8. The organic layer was washed with brine and dried over Na2SO4. After filtration and concentration, the crude product was purified by flash silica gel chromatography (50% EtOAc/hexanes) to give 151 mg of methyl 3-(azidomethyl)-5-(N-methylmethylsulfonamido)benzoate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299267B2
Source datasetuspto-grants-2012_10
ORD IDord-a5177ae5901349399e777fbf134f3567
Source noteuspto-grants-2012_10