HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453774Generated: October 30, 2026
Cyclohexyl bromide → HCID 67315056, compound
https://huagongshe.com/reaction/1453774
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexyl bromide | HCID 7960 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | 4-(5-Fluoro-2-methyl-1H-indol-3-yl)-2H-benzo[e][1,2,3]thiadiazine 1,1-dioxide | HCID 136388612 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67315056 | HCID 67315056 | — |
Reaction Steps
Cyclohexyl bromide (8 μL, 67 μmol) and K2CO3 (10 mg, 72 μmol) were added to a solution of 4-(5-fluoro-2-methyl-1H-indol-3-yl)-2H-benzo[e][1,2,3]thiadiazine 1,1-dioxide (20 mg, 61 μmol) in CH3CN (1 mL), and stirred overnight at 80° C. An additional amount of K2CO3 (10 mg, 72 μmol) and tert-butyl bromoacetate (14 μL, 92 μmol) was added, and the reaction mixture stirred an additional 2 h at 80° C. The reaction mixture was diluted with H2O and CH2Cl2, and filtered through an Extrelut column. The Extrelut column was washed with CH2Cl2, and the filtrate was concentrated to afford the sub-title compound, which was carried onto the next step without further purification or characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07476667B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-7661fd091e4a41059fa20c1be4ed06d0 |
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| Source note | uspto-grants-2009_01 |
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