HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326781Generated: October 30, 2026
Sodium Iodide → 6-Chloro-5-fluoro-2,3-dihydro-3-[(2-furoyl)oxy-(2-thienyl)methylene]-2-oxo-1H-indole-1-carboxamide
https://huagongshe.com/reaction/326781
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 2-Furancarbonyl chloride | HCID 68242 | — |
| Reactant | HCID 178514240 | HCID 178514240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Chloro-5-fluoro-2,3-dihydro-3-[(2-furoyl)oxy-(2-thienyl)methylene]-2-oxo-1H-indole-1-carboxamide | HCID 53832201 | — |
Reaction Steps
To a stirred suspension of (Z)- 6-chloro-5-fluoro-2,3-dihydro-3-(hydroxy-2-thienylmethylene)-2-oxo-1H-indole-1-carboxamide sodium salt (1.4 gm., 3.88 mmole) and sodium iodide (20 mg, 0.12 mmole) in 30 ml of dichloromethane was added 2-furoyl chloride (380 mg, 3.88 mmole). The resulting suspension was then stirred for 20 hr. at room temperature. The reaction suspension was filtered and washed with dichloromethane to remove unreacted 6-chloro-5-fluoro-2,3-dihydro-3-(hydroxy-2-thienylmethylene)-2-oxo-1H indole-1-carboxamide sodium salt. The filtrate was evaporated in vacuo to an orange solid which was chromatographed on a silica gel column (100 gm. silica gel) and eluted with dichloromethane to yield the crude titled compound as a solid. The solid was crystallized from dichloromethane and hexane to yield a yellow solid, 210 mg (12.6%): mp 215°-216° C. Anal. calcd. for C19H10ClFN2O5S: C, 52.73; H, 2.33; N, 6.47. Found: C, 52.66; H, 2.21; N, 6.46.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05270331 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-36b983ed13464d5a9983b86304ab6a11 |
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| Source note | uspto-grants-1993_12 |
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