HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237404Generated: October 28, 2026
Dimethylformamide → HCID 178437999, compound
https://huagongshe.com/reaction/237404
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Pentane | HCID 8003 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Reactant | HCID 178437989 | HCID 178437989 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178437999 | HCID 178437999 | — |
Reaction Steps
A solution of 6.90 g (30.7 mmol) 5-bromo-3-ethyl-1H-indazole (Example 7A) in THF (300 ml) was cooled to −78° C. At this temperature, a 1.7 M solution of tert-butyllithium in n-pentane (63.1 ml, 107 mmol) was slowly added. The mixture was stirred at −78° C. for 30 minutes before N,N-dimethylformamide (80.0 ml) was slowly added. The cooling bath was removed, and stirring was continued until room temperature was reached. Then, water (250 ml) was added carefully. The mixture was extracted several times with ethyl acetate (500 ml). The combined organic layers were washed with saturated aqueous sodium chloride solution, dried over sodium sulfate, and concentrated under reduced pressure to yield 4.5 g (84% of th.) of the crude title compound which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642595B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-88259785bac34dee90c55d7e96394b2b |
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| Source note | uspto-grants-2014_02 |
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