HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747504Generated: October 30, 2026
Diisopropylethylamine → HCID 178516596, compound
https://huagongshe.com/reaction/1747504
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Chloro-6-(trifluoromethyl)pyridazine | HCID 28242526 | — |
| Reactant | HCID 178479635 | HCID 178479635 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178516596 | HCID 178516596 | 30.2% |
Reaction Steps
N,N-Diisopropylethylamine (59.8 μL, 0.352 mmol) and 3-chloro-6-(trifluoromethyl)pyridazine (80.2 mg, 0.439 mmol) were added to a solution of 4-hydroxy-3-(piperidin-4-yl)-4-(trifluoromethyl)-1,4,5,7-tetrahydro-6H-pyrazolo[3,4-b]pyridin-6-one hydrochloride (100 mg, 0.293 mmol) produced in Reference Example 60 in dimethyl sulfoxide (0.5 mL), and the mixture was stirred overnight at room temperature. The reaction solution was diluted with ethyl acetate, washed with water, a saturated ammonium chloride aqueous solution, and brine in this order, and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography [elute: ethyl acetate/methanol=100/0-90/10 (gradient)] to obtain the title compound (39.8 mg, yield: 30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150575B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-0e7b5583eb664332b7f81ded0b72e539 |
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| Source note | uspto-grants-2015_10 |
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