HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592358Generated: October 27, 2026
Diethyl Ether → tert-Butyl 4-(4-((4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)-1H-pyrazol-1-yl)piperidine-1-carboxylate
https://huagongshe.com/reaction/592358
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Dichloro-5-(trifluoromethyl)pyrimidine | HCID 2782774 | — |
| Reactant | tert-butyl 4-(4-amino-1H-pyrazol-1-yl)piperidine-1-carboxylate | HCID 27281520 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | tert-Butyl 4-(4-((4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)-1H-pyrazol-1-yl)piperidine-1-carboxylate | HCID 86712281 | — |
Reaction Steps
A 1.0 M solution of ZnCl2 in Et2O (22.5 mL, 22.5 mmol) was added to a solution of 2,4-dichloro-5-(trifluoromethyl)pyrimidine (4.48 g, 20.7 mmol) in t-BuOH (50 mL) and DCE (50 mL) and the mixture was stirred for 10 minutes. The mixture was diluted with t-BuOH (50 mL) and DCE (50 mL) before tert-butyl 4-(4-amino-1H-pyrazol-1-yl)piperidine-1-carboxylate (5.00 g, 18.8 mmol) and Et3N (3.14 mL, 22.5 mmol) were added. Stirring was continued overnight and the volatiles were subsequently removed in vacuo. The resultant residue was suspended in acetone (50 mL) then water (500 mL) and sonicated for 15 minutes before the solid was removed by vacuum filtration and the filter cake washed with water (100 mL). The solid was suspended in acetone (25 mL), filtered and the filter cake was washed with petroleum benzine 40-60° C. (200 mL) to give the title compound K8 as a light pink solid (6.57 g, 78%). LCMS-D: rt 3.618 min; m/z 445.1 [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-ab16ab0db26040e691d0421d4e0843eb |
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| Source note | uspto-grants-2016_01 |
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