HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529782Generated: November 1, 2026
1,4-Dioxane hydrochloride → HCID 118522497, compound
https://huagongshe.com/reaction/529782
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Reactant | HCID 118523182 | HCID 118523182 | — |
| Product | HCID 118522497 | HCID 118522497 | 98.7% |
Reaction Steps
Saturated HCl dioxane solution (15 mL) was added to tert-butyl N-[1-(2-[3-[5-chloro-2-(difluoromethoxy)phenyl]-4-[pyrazolo[1,5-a]pyrimidine-3-amido]-1H-pyrazol-1-yl]ethyl)piperidin-4-yl]carbamate (400 mg, 0.63 mmol). The resulting solution was stirred at room temperature overnight and concentrated under vacuum. The pH value of the remaining solution was adjusted to 8-9 with saturated aqueous Na2CO3. The resulting mixture was concentrated under vacuum. The residue was purified by flash chromatography on silica eluting with MeOH/DCM (1:1) to afford 330 mg (98%) of N-[1-[2-(4-aminopiperidin-1-yl)ethyl]-3-[5-chloro-2-(difluoromethoxy)phenyl]-1H-pyrazol-4-yl]pyrazolo[1,5-a]pyrimidine-3-carboxamide as a yellow solid. LCMS (Method 28) [M+H]+=531.1, RT=0.49 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346815B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-1d0d0b6eed78456584e674d6046cd67e |
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| Source note | uspto-grants-2016_05 |
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