HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Aminocarbonylamino-6-azidomethylindole-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 2-Aminocarbonylamino-6-hydroxymethylindole-3-carboxamide | HCID 24989428 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Aminocarbonylamino-6-azidomethylindole-3-carboxamide | HCID 59189931 | 11.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08193237B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-44e89feb11b249e19d66e80b05704a5b |
| Source note | uspto-grants-2012_06 |