HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897472Generated: October 25, 2026
1-Bromo-3-chloropropane → 6-(3-Chloropropoxy)-5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazole
https://huagongshe.com/reaction/1897472
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazol-6-ol | HCID 136163662 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-(3-Chloropropoxy)-5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazole | HCID 67410626 | — |
Reaction Steps
To a solution of 5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazol-6-ol (0.015 g, 0.05 mmol) in DMF (1 mL) was added Cs2CO3. The reaction mixture was stirred for 30 minutes before the addition of 1-bromo-3-chloropropane (0.01 g, 0.08 mmol) and then was heated to 80° C. for 25 hours. After cooling the mixture to room temperature, the reaction mixture was diluted with water and ether and the layers separated. The aqueous layer was extracted with ether and the combined organic layers were washed with 1N NaOH, water, and brine. The crude mixture was dried over Na2SO4 and concentrated under reduced pressure to afford the product with a small impurity. The crude mixture was used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518983B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-fffee2b82dfd42d9b41cf7503a029eb1 |
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| Source note | uspto-grants-2013_08 |
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