HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730419Generated: October 30, 2026
Dimethylformamide → HCID 86760949, compound
https://huagongshe.com/reaction/730419
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | HCID 69061514 | HCID 69061514 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86760949 | HCID 86760949 | — |
Reaction Steps
To a solution of diisopropylamine (3.72 ml, 28.4 mmol) in tetrahydrofuran (36 ml) was added a 1.6 N solution of butyllithium in hexane (17.7 ml, 28.4 mmol) at −78° C., and the mixture was stirred at −78° C. for 15 minutes. To the resultant solution was added dropwise 4,6-dimethyl-1-[(1R)-1,2,3,4-tetrahydronaphthalen-1-yl]-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile (5.70 g, 18.9 mmol) in THF (60 ml) at −78° C., and the mixture was stirred at −78° C. for 30 minutes. Dimethylformamide (5.37 ml, 56.7 mmol) was added thereto, and the mixture was stirred at room temperature 1.5 hours, poured into iced water, and extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to give the objective product as oily matter.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582651B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-7851c3a0bb1d4819b32254ee0b673126 |
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| Source note | uspto-grants-2009_09 |
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