HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 18007587, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-(Thiophen-3-yl)-1H-indazole | HCID 18007497 | — |
| Reactant | HCID 22612932 | HCID 22612932 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18007527 | HCID 18007527 | 28% |
| Product | HCID 18007587 | HCID 18007587 | 63% |
Reaction Steps
1-(3-chloropropyl)-6-(3-thienyl)-1H-indazole 1-chloro-3-iodopropane (0.14 mL, 1.3 mmol) was added to a DMF (3 mL) solution of 6-(3-thienyl)-1H-indazole (88.4 mg, 0.44 mmol) and sodium hydride (60%, 72 mg, 1.8 mmol) that had been allowed to stir for 5 min at room temperature under argon. The reaction mixture was allowed to stir at room temperature overnight before quenching with brine (20 mL) and partitioning into ethyl acetate (100 mL), and drying over anhydrous sodium sulfate. The solvent was removed in vacuo and flash chromatography (silica gel, 10-20% ethyl acetate in hexane) yielded 1-(3-chloropropyl)-6-(3-thienyl)-1H-indazole (76.6 mg, 63%) as well as the side product 2-(3-chloropropyl)-6-(3-thienyl)-2H-indazole (33.9 mg, 28%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06380242B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-29b9d96453f743dd99baafe3c54c9106 |
| Source note | uspto-grants-2002_04 |