HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride → 5,6-difluoro-3-iodo-1-(phenylsulfonyl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5,6-difluoro-3-iodo-1H-indole | HCID 118060416 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5,6-difluoro-3-iodo-1-(phenylsulfonyl)-1H-indole | HCID 118060283 | 72.4% |
Reaction Steps
To a solution of 5,6-difluoro-3-iodo-1H-indole (Intermediate 27; 930 mg; 3.33 mmol) in THF (20 mL) at 0° C. was added NaH (266.4 mg; 60%; 6.66 mmol) under nitrogen. The reaction mixture was stirred at r.t. for 15 minutes before a solution of benzenesulfonyl chloride (763.4 mg; 4.32 mmol) in THF (2 mL) was added dropwise. The reaction was stirred at r.t. for 12 hours, quenched with an ice-water mixture (60 mL) and extracted with EtOAc (30 mL×3). The combined organic layers were washed with brine (100 mL), dried over anhydrous Na2SO4, filtered, concentrated, and purified by a silica gel chromatography (petroleum ether/EtOAc=10/1-3/1) to afford 1.01 g (72%) of the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09126984B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-d1f273ecb1fa4caa8ad0d1150e364d70 |
| Source note | uspto-grants-2015_09 |