HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride → HCID 86661597, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 66707411 | HCID 66707411 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 86661597 | HCID 86661597 | — |
Reaction Steps
Under an argon atmosphere [1-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-cyclopropylmethyl]-carbamic acid cyclopentyl ester was mixed with N-iodosuccinimide. BF3*2H2O was added at 0° C. The dark suspension was stirred at rt for 3 h after which it was poured onto a 1:1 solution of saturated Na2S2O3 and saturated NaHCO3 (20 mL). The aqueous phase was extracted with DCM (×2) and the combined organic phases were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude product was purified by flash chromatography on silica to afford [1-(5-Iodo-8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-cyclopropylmethyl]-carbamic acid cyclopentyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952162B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-07b10d6ae6754d6e981c79cfeaab64b9 |
| Source note | uspto-grants-2015_02 |