Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 57749236 | HCID 57749236 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57387081 | HCID 57387081 | 31.5% |
Reaction Steps
A mixture of 3-({2-[(cyclopropylcarbonyl)amino][1,3]thiazolo[5,4-b]pyridin-5-yl}oxy)benzoic acid (3.90 g, 11.0 mmol), diphenylphosphoryl azide (3.55 mL, 16.5 mmol), triethylamine (2.28 mL, 16.5 mmol) and N,N-dimethylformamide (80 mL) was stirred at room temperature for 3 hr, and water (20 mL) was added and the mixture was stirred at 100° C. for 15 hr. The precipitation solid was collected by filtration. 6N Hydrochloric acid (100 mL), ethyl acetate (30 mL) and tetrahydrofuran (10 mL) were added to the solid, and the mixture was stirred at room temperature for 30 min. The insoluble material was filtered off, and the aqueous layer was separated from the filtrate, neutralized with 8N aqueous sodium hydroxide solution, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was collected by filtration and washed with ethyl acetate-hexane to give the title compound (1.13 g, 31%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08304557B2 |
|---|
| Source dataset | uspto-grants-2012_11 |
|---|
| ORD ID | ord-42f6dcb2bc254f4098960593eed4c64a |
|---|
| Source note | uspto-grants-2012_11 |
|---|