HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465711Generated: November 1, 2026
Potassium Carbonate → tert-butyl 3-(1-(3-(pyridin-4-yl)-1-trityl-1H-indazol-5-yl)-1H-pyrazol-3-yl)piperidine-1-carboxylate
https://huagongshe.com/reaction/1465711
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (1R,2R)-N1,N1-Dimethylcyclohexane-1,2-diamine | HCID 11275066 | — |
| Reactant | 5-iodo-3-(pyridin-4-yl)-1-trityl-1H-indazole | HCID 67518146 | — |
| Reactant | HCID 178451848 | HCID 178451848 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-butyl 3-(1-(3-(pyridin-4-yl)-1-trityl-1H-indazol-5-yl)-1H-pyrazol-3-yl)piperidine-1-carboxylate | HCID 67518079 | 110.7% |
Reaction Steps
The mixture of 5-iodo-3-(pyridin-4-yl)-1-trityl-1H-indazole (281 mg, 0.5 mmol), tert-butyl 3-(1H-pyrazol-3-yl)piperidine-1-carboxylate (151 mg, 0.6 mmol), copper (I) iodide (19 mg, 0.1 mmol), rac-trans-N,N-dimethylcyclohexane-1,2-diamine (57 mg, 0.4 mmol), K2CO3 (552 mg, 4 mmol) in toluene (3 mL) was heated at 100° C. for 4 days. After cooling to room temperature, the reaction mixture was filtered through a pad of celite, and washed with EtOAc. The filtrate was concentrated and column purified with mixture of methanol, dichloromethane and ammonia to give tert-butyl 3-(1-(3-(pyridin-4-yl)-1-trityl-1H-indazol-5-yl)-1H-pyrazol-3-yl)piperidine-1-carboxylate (380 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999966B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-ddaab4b32d164d4ba61cb8f0088256f9 |
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| Source note | uspto-grants-2015_04 |
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