HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601756Generated: October 29, 2026
Benzothiazole → 3-Benzothiazol-2-yl-5-chloro-3-hydroxy-1,3-dihydroindol-2-one
https://huagongshe.com/reaction/601756
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzothiazole | HCID 7222 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-chloro-1H-indole-2,3-dione | HCID 87203 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Benzothiazol-2-yl-5-chloro-3-hydroxy-1,3-dihydroindol-2-one | HCID 57517750 | 70.6% |
Reaction Steps
A 1.6 M solution of n-butyllithium in hexane (35 ml, 56 mmol) was added dropwise to a solution of benzothiazole (6.2 ml, 56 mmol) in THF (100 ml) at −78° C. After stirring at −78° C. for 1.5 h, the solution of the lithiated benzothiazole was transferred via a needle into an ice-cold suspension of 5-chloroisatin (3.63 g, 20 mmol) in THF (70 ml). The reaction mixture was stirred at 0° C. for 1 h and then saturated ammonium chloride solution was added. The mixture was extracted three times with ethyl acetate and the combined organic layers were washed with saturated brine. The organic phase was dried over magnesium sulfate, filtered and concentrated under reduced pressure, during which the intermediate starts to crystallize. Filtration and drying yielded 4.47 g of the intermediate as yellow crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902379B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-d5b4259c52af42ddaf18e69ac2ea94c4 |
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| Source note | uspto-grants-2011_03 |
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