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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216642Generated: October 30, 2026

Water → 2-Aminocarbonylamino-6-azidomethylindole-3-carboxamide

https://huagongshe.com/reaction/216642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2-Aminocarbonylamino-6-hydroxymethylindole-3-carboxamideHCID 24989428—
SolventTetrahydrofuranHCID 8028—
Product2-Aminocarbonylamino-6-azidomethylindole-3-carboxamideHCID 5918993111.4%

Reaction Steps

Diphenylphosphoryl azide (42 μL, 0.19 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (29 μL, 0.19 mmol) were added to a solution of 2-aminocarbonylamino-6-hydroxymethylindole-3-carboxamide (Compound 16-1, 40 mg, 0.16 mmol) in anhydrous tetrahydrofuran (5 mL) under ice-cooling, the mixture was stirred at room temperature overnight. Water (10 mL) was added to the reaction mixture, and the whole was extracted with ethyl acetate (10 mL). The organic layer was washed with brine (20 mL) and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the title compound (5.0 mg) as a yellow solid (yield 11%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193237B2
Source datasetuspto-grants-2012_06
ORD IDord-44e89feb11b249e19d66e80b05704a5b
Source noteuspto-grants-2012_06