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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | Methyl 3-(hydroxymethyl)-5-[methyl(methylsulfonyl)amino]benzoate | HCID 57815142 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl 3-(azidomethyl)-5-(N-methylmethylsulfonamido)benzoate | HCID 86647414 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299267B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-a5177ae5901349399e777fbf134f3567 |
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| Source note | uspto-grants-2012_10 |
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