HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592484Generated: October 31, 2026
HCID 86712347, compound → HCID 86712346, compound
https://huagongshe.com/reaction/592484
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86712347 | HCID 86712347 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86712346 | HCID 86712346 | — |
Reaction Steps
A mixture of tert-butyl 4-(4-((4-((2-(1-carbamoylcyclopropyl)phenyl)ethynyl)-5-(trifluoromethyl)pyrimidin-2-yl)amino)-1H-pyrazol-1-yl)piperidine-1-carboxylate A76 (0.405 g, 0.680 mmol) and 10% Pd/C (wetted with ca. 53% water, 0.200 g) in EtOAc (30 mL) and MeOH (15 mL) was stirred under an atmosphere of H2 at room temperature for 16 hours. The mixture was filtered through a plug of Celite and the filtrate was concentrated in vacuo. Purification by column chromatography (Biotage Isolera, 40 g SiO2 cartridge, 0-10% MeOH in DCM) gave a yellow oil which was further purified by column chromatography (Biotage Isolera, 40 g SiO2 cartridge, 10-90% EtOAc in petroleum benzine 40-60° C.) to give the title compound A77 as a yellow solid (0.213 g, 52%). LCMS-D: rt 3.62 min; m/z 600 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238644B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-4065b19706534c0bb7a5a6bbe8892484 |
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| Source note | uspto-grants-2016_01 |
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